Canonical Allele Identifier: CA619266167
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1372250264
gnomAD v2: 15-80445050-A-C
gnomAD v3: 15-80152708-A-C
gnomAD v4: 15-80152708-A-C
MyVariant Identifiers: chr15:g.80445050A>C (hg19) chr15:g.80152708A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152708A>C , CM000677.2:g.80152708A>C GRCh38
NC_000015.9:g.80445050A>C , CM000677.1:g.80445050A>C GRCh37
NC_000015.8:g.78232105A>C NCBI36
NG_012833.1:g.4710A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-30+163A>C ENSP00000453152.1:n.-30+163A>C
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