Canonical Allele Identifier: CA491688112

Gene: FAH

Linked Data

• dbSNP Id: rs11555096
• gnomAD v3: 15-80180184-C-A
• gnomAD v4: 15-80180184-C-A
• MyVariant Identifiers: chr15:g.80472526C>A (hg19) ; chr15:g.80180184C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180184C>A , CM000677.2:g.80180184C>A	GRCh38
NC_000015.9:g.80472526C>A , CM000677.1:g.80472526C>A	GRCh37
NC_000015.8:g.78259581C>A	NCBI36
NG_012833.1:g.32186C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.1110C>A
ENST00000561421.6:c.1021C>A MANE Select	ENSP00000453347.2:p.Arg341=
ENST00000646551.1:n.2635C>A
ENST00000261755.9:c.1021C>A	ENSP00000261755.5:p.Arg341=
ENST00000407106.5:c.1021C>A	ENSP00000385080.1:p.Arg341=
ENST00000539156.5:c.811C>A	ENSP00000454271.1:p.Arg271=
ENST00000559217.1:n.238C>A
ENST00000561353.2:c.119C>A
ENST00000561421.5:c.1021C>A	ENSP00000453347.1:p.Arg341=
NM_000137.2:c.1021C>A	NP_000128.1:p.Arg341=
XM_024449872.1:c.1021C>A	XP_024305640.1:p.Arg341=
NM_000137.4:c.1021C>A MANE Select	NP_000128.1:p.Arg341=
NM_001374377.1:c.1021C>A	NP_001361306.1:p.Arg341=
NM_001374380.1:c.1021C>A	NP_001361309.1:p.Arg341=