Canonical Allele Identifier: CA971893026
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs1181908136
gnomAD v3: 15-80152496-G-T
gnomAD v4: 15-80152496-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152496G>T , CM000677.2:g.80152496G>T GRCh38
NC_000015.9:g.80444838G>T , CM000677.1:g.80444838G>T GRCh37
NC_000015.8:g.78231893G>T NCBI36
NG_012833.1:g.4498G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558022.5:c.-79G>T ENSP00000453152.1:n.-79G>T
Search 100 bp 5'
Search 100 bp 3'