Canonical Allele Identifier: CA274021557

Gene: FAH

Linked Data

• dbSNP Id: rs576942274
• gnomAD v3: 15-80162552-A-G
• gnomAD v4: 15-80162552-A-G
• MyVariant Identifiers: chr15:g.80454894A>G (hg19) ; chr15:g.80162552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80162552A>G , CM000677.2:g.80162552A>G	GRCh38
NC_000015.9:g.80454894A>G , CM000677.1:g.80454894A>G	GRCh37
NC_000015.8:g.78241949A>G	NCBI36
NG_012833.1:g.14554A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.*188A>G	ENSP00000507680.1:n.*188A>G
ENST00000682012.1:n.530+216A>G
ENST00000683593.1:n.2334A>G
ENST00000684363.1:c.525A>G	ENSP00000507314.1:n.525A>G
ENST00000684569.1:n.500+216A>G
ENST00000561421.6:c.455+216A>G MANE Select	ENSP00000453347.2:n.455+216A>G
ENST00000646551.1:n.1942+216A>G
ENST00000261755.9:c.455+216A>G	ENSP00000261755.5:n.455+216A>G
ENST00000407106.5:c.455+216A>G	ENSP00000385080.1:n.455+216A>G
ENST00000537726.5:n.817A>G
ENST00000539156.5:c.245+216A>G	ENSP00000454271.1:n.245+216A>G
ENST00000558022.5:c.455+216A>G	ENSP00000453152.1:n.455+216A>G
ENST00000558627.1:n.383+216A>G
ENST00000558767.5:n.932A>G
ENST00000561421.5:c.455+216A>G	ENSP00000453347.1:n.455+216A>G
NM_000137.2:c.455+216A>G	NP_000128.1:n.455+216A>G
XM_024449872.1:c.455+216A>G	XP_024305640.1:n.455+216A>G
NM_000137.4:c.455+216A>G MANE Select	NP_000128.1:n.455+216A>G
NM_001374377.1:c.455+216A>G	NP_001361306.1:n.455+216A>G
NM_001374380.1:c.455+216A>G	NP_001361309.1:n.455+216A>G