Canonical Allele Identifier: CA7691269

Gene: FAH

Linked Data

• dbSNP Id: rs373558223
• ExAC: 15:80460704 G / A
• gnomAD v2: 15-80460704-G-A
• gnomAD v3: 15-80168362-G-A
• gnomAD v4: 15-80168362-G-A
• MyVariant Identifiers: chr15:g.80460704G>A (hg19) ; chr15:g.80168362G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168362G>A , CM000677.2:g.80168362G>A	GRCh38
NC_000015.9:g.80460704G>A , CM000677.1:g.80460704G>A	GRCh37
NC_000015.8:g.78247759G>A	NCBI36
NG_012833.1:g.20364G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.795+46G>A
ENST00000684569.1:n.651+46G>A
ENST00000561421.6:c.606+46G>A MANE Select	ENSP00000453347.2:n.606+46G>A
ENST00000646551.1:n.2233+46G>A
ENST00000261755.9:c.606+46G>A	ENSP00000261755.5:n.606+46G>A
ENST00000407106.5:c.606+46G>A	ENSP00000385080.1:n.606+46G>A
ENST00000539156.5:c.396+46G>A	ENSP00000454271.1:n.396+46G>A
ENST00000558514.1:n.198G>A
ENST00000558627.1:n.534+46G>A
ENST00000561421.5:c.606+46G>A	ENSP00000453347.1:n.606+46G>A
NM_000137.2:c.606+46G>A	NP_000128.1:n.606+46G>A
XM_024449872.1:c.606+46G>A	XP_024305640.1:n.606+46G>A
NM_000137.4:c.606+46G>A MANE Select	NP_000128.1:n.606+46G>A
NM_001374377.1:c.606+46G>A	NP_001361306.1:n.606+46G>A
NM_001374380.1:c.606+46G>A	NP_001361309.1:n.606+46G>A