Canonical Allele Identifier: CA619266124
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1487645227
gnomAD v2: 15-80444837-A-G
gnomAD v3: 15-80152495-A-G
gnomAD v4: 15-80152495-A-G
MyVariant Identifiers: chr15:g.80444837A>G (hg19) chr15:g.80152495A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152495A>G , CM000677.2:g.80152495A>G GRCh38
NC_000015.9:g.80444837A>G , CM000677.1:g.80444837A>G GRCh37
NC_000015.8:g.78231892A>G NCBI36
NG_012833.1:g.4497A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-80A>G ENSP00000453152.1:n.-80A>G
Search 100 bp 5'
Search 100 bp 3'