Canonical Allele Identifier: CA716102598

Gene: FAH

Linked Data

• dbSNP Id: rs1339650134
• gnomAD v3: 15-80152856-C-T
• gnomAD v4: 15-80152856-C-T
• MyVariant Identifiers: chr15:g.80445198C>T (hg19) ; chr15:g.80152856C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152856C>T , CM000677.2:g.80152856C>T	GRCh38
NC_000015.9:g.80445198C>T , CM000677.1:g.80445198C>T	GRCh37
NC_000015.8:g.78232253C>T	NCBI36
NG_012833.1:g.4858C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-199C>T	ENSP00000507680.1:n.-199C>T
ENST00000261755.9:c.-30+15C>T	ENSP00000261755.5:n.-30+15C>T
ENST00000407106.5:c.-79C>T	ENSP00000385080.1:n.-79C>T
ENST00000537726.5:n.53+15C>T
ENST00000558022.5:c.-29-170C>T	ENSP00000453152.1:n.-29-170C>T
ENST00000558767.5:n.63C>T
ENST00000561369.1:n.2C>T
XM_024449872.1:c.-79C>T	XP_024305640.1:n.-79C>T
NM_001374377.1:c.-79C>T	NP_001361306.1:n.-79C>T
NM_001374380.1:c.-30+15C>T	NP_001361309.1:n.-30+15C>T