Canonical Allele Identifier: CA2629872846

Gene: FAH

Linked Data

• gnomAD v4: 15-80152828-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152828T>A , CM000677.2:g.80152828T>A	GRCh38
NC_000015.9:g.80445170T>A , CM000677.1:g.80445170T>A	GRCh37
NC_000015.8:g.78232225T>A	NCBI36
NG_012833.1:g.4830T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-227T>A	ENSP00000507680.1:n.-227T>A
ENST00000261755.9:c.-43T>A	ENSP00000261755.5:n.-43T>A
ENST00000407106.5:c.-107T>A	ENSP00000385080.1:n.-107T>A
ENST00000537726.5:n.40T>A
ENST00000558022.5:c.-29-198T>A	ENSP00000453152.1:n.-29-198T>A
ENST00000558767.5:n.35T>A
XM_024449872.1:c.-107T>A	XP_024305640.1:n.-107T>A
NM_001374377.1:c.-107T>A	NP_001361306.1:n.-107T>A
NM_001374380.1:c.-43T>A	NP_001361309.1:n.-43T>A