Canonical Allele Identifier: CA2629872979

Gene: FAH

Linked Data

• gnomAD v4: 15-80152902-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152902T>A , CM000677.2:g.80152902T>A	GRCh38
NC_000015.9:g.80445244T>A , CM000677.1:g.80445244T>A	GRCh37
NC_000015.8:g.78232299T>A	NCBI36
NG_012833.1:g.4904T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-153T>A	ENSP00000507680.1:n.-153T>A
ENST00000261755.9:c.-30+61T>A	ENSP00000261755.5:n.-30+61T>A
ENST00000407106.5:c.-33T>A	ENSP00000385080.1:n.-33T>A
ENST00000537726.5:n.53+61T>A
ENST00000558022.5:c.-29-124T>A	ENSP00000453152.1:n.-29-124T>A
ENST00000558767.5:n.109T>A
ENST00000561369.1:n.48T>A
ENST00000561421.5:c.-153T>A	ENSP00000453347.1:n.-153T>A
NM_000137.2:c.-153T>A	NP_000128.1:n.-153T>A
XM_024449872.1:c.-33T>A	XP_024305640.1:n.-33T>A
NM_001374377.1:c.-33T>A	NP_001361306.1:n.-33T>A
NM_001374380.1:c.-30+61T>A	NP_001361309.1:n.-30+61T>A