Canonical Allele Identifier: CA716102354
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1381237630
gnomAD v3: 15-80152520-A-T
gnomAD v4: 15-80152520-A-T
MyVariant Identifiers: chr15:g.80444862A>T (hg19) chr15:g.80152520A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152520A>T , CM000677.2:g.80152520A>T GRCh38
NC_000015.9:g.80444862A>T , CM000677.1:g.80444862A>T GRCh37
NC_000015.8:g.78231917A>T NCBI36
NG_012833.1:g.4522A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-55A>T ENSP00000453152.1:n.-55A>T
Search 100 bp 5'
Search 100 bp 3'