Canonical Allele Identifier: CA716102650

Gene: FAH

Linked Data

• dbSNP Id: rs1358137303
• gnomAD v3: 15-80152918-G-A
• gnomAD v4: 15-80152918-G-A
• MyVariant Identifiers: chr15:g.80445260G>A (hg19) ; chr15:g.80152918G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152918G>A , CM000677.2:g.80152918G>A	GRCh38
NC_000015.9:g.80445260G>A , CM000677.1:g.80445260G>A	GRCh37
NC_000015.8:g.78232315G>A	NCBI36
NG_012833.1:g.4920G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-137G>A	ENSP00000507680.1:n.-137G>A
ENST00000261755.9:c.-30+77G>A	ENSP00000261755.5:n.-30+77G>A
ENST00000407106.5:c.-30+13G>A	ENSP00000385080.1:n.-30+13G>A
ENST00000537726.5:n.53+77G>A
ENST00000558022.5:c.-29-108G>A	ENSP00000453152.1:n.-29-108G>A
ENST00000558767.5:n.125G>A
ENST00000561369.1:n.51+13G>A
ENST00000561421.5:c.-137G>A	ENSP00000453347.1:n.-137G>A
NM_000137.2:c.-137G>A	NP_000128.1:n.-137G>A
XM_024449872.1:c.-30+13G>A	XP_024305640.1:n.-30+13G>A
NM_001374377.1:c.-30+13G>A	NP_001361306.1:n.-30+13G>A
NM_001374380.1:c.-30+77G>A	NP_001361309.1:n.-30+77G>A