{{Rsnum
|rsid=387906472
|Chromosome=X
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AGTG)
|geno3=(AGTG;AGTG)
|Gene=ALAS2
|position=55009235
|Gene_s=ALAS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000011228.5
|CLNALLE=1
|CLNDBN=Protoporphyria, erythropoietic, X-linked
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK121284:C2677889:300752:79278
|CLNHGVS=NC_000023.10:g.55035668_55035671delCACT
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK121284; 301300.0015
|Disease=Protoporphyria
|FwdREF=AGTG
|REF=CCACT
|RSPOS=55035667
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906472
|GENEINFO=ALAS2:212
|GENE_ID=212
|GENE_NAME=ALAS2
}}