Canonical Allele Identifier: CA619271337

Gene: FAH

Linked Data

• dbSNP Id: rs1186550809
• gnomAD v2: 15-80472085-A-G
• gnomAD v3: 15-80179743-A-G
• gnomAD v4: 15-80179743-A-G
• MyVariant Identifiers: chr15:g.80472085A>G (hg19) ; chr15:g.80179743A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80179743A>G , CM000677.2:g.80179743A>G	GRCh38
NC_000015.9:g.80472085A>G , CM000677.1:g.80472085A>G	GRCh37
NC_000015.8:g.78259140A>G	NCBI36
NG_012833.1:g.31745A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1050-381A>G
ENST00000561421.6:c.961-381A>G MANE Select	ENSP00000453347.2:n.961-381A>G
ENST00000646551.1:n.2575-381A>G
ENST00000261755.9:c.961-381A>G	ENSP00000261755.5:n.961-381A>G
ENST00000407106.5:c.961-381A>G	ENSP00000385080.1:n.961-381A>G
ENST00000539156.5:c.751-381A>G	ENSP00000454271.1:n.751-381A>G
ENST00000559217.1:n.178-381A>G
ENST00000561353.2:c.59-381A>G
ENST00000561421.5:c.961-381A>G	ENSP00000453347.1:n.961-381A>G
NM_000137.2:c.961-381A>G	NP_000128.1:n.961-381A>G
XM_024449872.1:c.961-381A>G	XP_024305640.1:n.961-381A>G
NM_000137.4:c.961-381A>G MANE Select	NP_000128.1:n.961-381A>G
NM_001374377.1:c.961-381A>G	NP_001361306.1:n.961-381A>G
NM_001374380.1:c.961-381A>G	NP_001361309.1:n.961-381A>G