Canonical Allele Identifier: CA491682780

Gene: FAH

Linked Data

• ClinVar Variation Id: 1633838
• ClinVar RCV Id: RCV002124200
• dbSNP Id: rs149988384
• MyVariant Identifiers: chr15:g.80460616C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168274C>G , CM000677.2:g.80168274C>G	GRCh38
NC_000015.9:g.80460616C>G , CM000677.1:g.80460616C>G	GRCh37
NC_000015.8:g.78247671C>G	NCBI36
NG_012833.1:g.20276C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.753C>G
ENST00000684569.1:n.609C>G
ENST00000561421.6:c.564C>G MANE Select	ENSP00000453347.2:p.Pro188=
ENST00000646551.1:n.2191C>G
ENST00000261755.9:c.564C>G	ENSP00000261755.5:p.Pro188=
ENST00000407106.5:c.564C>G	ENSP00000385080.1:p.Pro188=
ENST00000539156.5:c.354C>G	ENSP00000454271.1:p.Pro118=
ENST00000558514.1:n.110C>G
ENST00000558627.1:n.492C>G
ENST00000561421.5:c.564C>G	ENSP00000453347.1:p.Pro188=
NM_000137.2:c.564C>G	NP_000128.1:p.Pro188=
XM_024449872.1:c.564C>G	XP_024305640.1:p.Pro188=
NM_000137.4:c.564C>G MANE Select	NP_000128.1:p.Pro188=
NM_001374377.1:c.564C>G	NP_001361306.1:p.Pro188=
NM_001374380.1:c.564C>G	NP_001361309.1:p.Pro188=