Canonical Allele Identifier: CA730576

Gene: FABP3

Linked Data

• dbSNP Id: rs759645576
• ExAC: 1:31845811 G / A
• gnomAD v2: 1-31845811-G-A
• gnomAD v4: 1-31372964-G-A
• COSMIC: COSM908152
• MyVariant Identifiers: chr1:g.31845811G>A (hg19) ; chr1:g.31372964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31372964G>A , CM000663.2:g.31372964G>A	GRCh38
NC_000001.10:g.31845811G>A , CM000663.1:g.31845811G>A	GRCh37
NC_000001.9:g.31618398G>A	NCBI36
NG_047049.1:g.5320C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.51C>T MANE Select	ENSP00000362817.2:p.Phe17=
ENST00000373713.6:c.51C>T	ENSP00000362817.2:p.Phe17=
ENST00000482018.1:c.51C>T	ENSP00000473982.1:p.Phe17=
ENST00000498148.5:c.51C>T	ENSP00000474078.1:p.Phe17=
NM_004102.3:c.51C>T	NP_004093.1:p.Phe17=
XM_011541007.1:c.51C>T	XP_011539309.1:p.Phe17=
NM_001320996.1:c.51C>T	NP_001307925.1:p.Phe17=
NM_004102.4:c.51C>T	NP_004093.1:p.Phe17=
XM_011541007.3:c.51C>T	XP_011539309.1:p.Phe17=
NM_004102.5:c.51C>T MANE Select	NP_004093.1:p.Phe17=
NM_001320996.2:c.51C>T	NP_001307925.1:p.Phe17=