Canonical Allele Identifier: CA7691413

Gene: FAH

Linked Data

• dbSNP Id: rs758975576
• ExAC: 15:80469958 G / A
• gnomAD v2: 15-80469958-G-A
• gnomAD v4: 15-80177616-G-A
• MyVariant Identifiers: chr15:g.80469958G>A (hg19) ; chr15:g.80177616G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80177616G>A , CM000677.2:g.80177616G>A	GRCh38
NC_000015.9:g.80469958G>A , CM000677.1:g.80469958G>A	GRCh37
NC_000015.8:g.78257013G>A	NCBI36
NG_012833.1:g.29618G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1049+33G>A
ENST00000561421.6:c.960+33G>A MANE Select	ENSP00000453347.2:n.960+33G>A
ENST00000646551.1:n.2574+33G>A
ENST00000261755.9:c.960+33G>A	ENSP00000261755.5:n.960+33G>A
ENST00000407106.5:c.960+33G>A	ENSP00000385080.1:n.960+33G>A
ENST00000539156.5:c.750+33G>A	ENSP00000454271.1:n.750+33G>A
ENST00000559217.1:n.177+33G>A
ENST00000561353.2:c.58+33G>A
ENST00000561421.5:c.960+33G>A	ENSP00000453347.1:n.960+33G>A
NM_000137.2:c.960+33G>A	NP_000128.1:n.960+33G>A
XM_024449872.1:c.960+33G>A	XP_024305640.1:n.960+33G>A
NM_000137.4:c.960+33G>A MANE Select	NP_000128.1:n.960+33G>A
NM_001374377.1:c.960+33G>A	NP_001361306.1:n.960+33G>A
NM_001374380.1:c.960+33G>A	NP_001361309.1:n.960+33G>A