Canonical Allele Identifier: CA339578398

Gene: FABP3

Linked Data

• dbSNP Id: rs1387660539
• gnomAD v2: 1-31845806-T-A
• gnomAD v3: 1-31372959-T-A
• gnomAD v4: 1-31372959-T-A
• MyVariant Identifiers: chr1:g.31845806T>A (hg19) ; chr1:g.31372959T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31372959T>A , CM000663.2:g.31372959T>A	GRCh38
NC_000001.10:g.31845806T>A , CM000663.1:g.31845806T>A	GRCh37
NC_000001.9:g.31618393T>A	NCBI36
NG_047049.1:g.5325A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.56A>T MANE Select	ENSP00000362817.2:p.Asp19Val
ENST00000373713.6:c.56A>T	ENSP00000362817.2:p.Asp19Val
ENST00000482018.1:c.56A>T	ENSP00000473982.1:p.Asp19Val
ENST00000498148.5:c.56A>T	ENSP00000474078.1:p.Asp19Val
NM_004102.3:c.56A>T	NP_004093.1:p.Asp19Val
XM_011541007.1:c.56A>T	XP_011539309.1:p.Asp19Val
NM_001320996.1:c.56A>T	NP_001307925.1:p.Asp19Val
NM_004102.4:c.56A>T	NP_004093.1:p.Asp19Val
XM_011541007.3:c.56A>T	XP_011539309.1:p.Asp19Val
NM_004102.5:c.56A>T MANE Select	NP_004093.1:p.Asp19Val
NM_001320996.2:c.56A>T	NP_001307925.1:p.Asp19Val