Canonical Allele Identifier: CA7691285

Gene: FAH

Linked Data

• dbSNP Id: rs76497285
• ExAC: 15:80464493 T / G
• gnomAD v2: 15-80464493-T-G
• gnomAD v4: 15-80172151-T-G
• MyVariant Identifiers: chr15:g.80464493T>G (hg19) ; chr15:g.80172151T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80172151T>G , CM000677.2:g.80172151T>G	GRCh38
NC_000015.9:g.80464493T>G , CM000677.1:g.80464493T>G	GRCh37
NC_000015.8:g.78251548T>G	NCBI36
NG_012833.1:g.24153T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.796-863T>G
ENST00000561421.6:c.609T>G MANE Select	ENSP00000453347.2:p.Ala203=
ENST00000646551.1:n.2234-11T>G
ENST00000261755.9:c.609T>G	ENSP00000261755.5:p.Ala203=
ENST00000407106.5:c.609T>G	ENSP00000385080.1:p.Ala203=
ENST00000539156.5:c.399T>G	ENSP00000454271.1:p.Ala133=
ENST00000558627.1:n.537T>G
ENST00000561421.5:c.609T>G	ENSP00000453347.1:p.Ala203=
NM_000137.2:c.609T>G	NP_000128.1:p.Ala203=
XM_024449872.1:c.609T>G	XP_024305640.1:p.Ala203=
NM_000137.4:c.609T>G MANE Select	NP_000128.1:p.Ala203=
NM_001374377.1:c.609T>G	NP_001361306.1:p.Ala203=
NM_001374380.1:c.609T>G	NP_001361309.1:p.Ala203=