Canonical Allele Identifier: CA730601

Gene: FABP3

Linked Data

• dbSNP Id: rs373379949
• ExAC: 1:31845912 G / T
• gnomAD v2: 1-31845912-G-T
• MyVariant Identifiers: chr1:g.31845912G>T (hg19) ; chr1:g.31373065G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31373065G>T , CM000663.2:g.31373065G>T	GRCh38
NC_000001.10:g.31845912G>T , CM000663.1:g.31845912G>T	GRCh37
NC_000001.9:g.31618499G>T	NCBI36
NG_047049.1:g.5219C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.-51C>A MANE Select	ENSP00000362817.2:n.-51C>A
ENST00000373713.6:c.-51C>A	ENSP00000362817.2:n.-51C>A
ENST00000482018.1:c.-27-24C>A	ENSP00000473982.1:n.-27-24C>A
ENST00000498148.5:c.-51C>A	ENSP00000474078.1:n.-51C>A
NM_004102.3:c.-51C>A	NP_004093.1:n.-51C>A
XM_011541007.1:c.-51C>A	XP_011539309.1:n.-51C>A
NM_001320996.1:c.-51C>A	NP_001307925.1:n.-51C>A
NM_004102.4:c.-51C>A	NP_004093.1:n.-51C>A
XM_011541007.3:c.-51C>A	XP_011539309.1:n.-51C>A
NM_004102.5:c.-51C>A MANE Select	NP_004093.1:n.-51C>A
NM_001320996.2:c.-51C>A	NP_001307925.1:n.-51C>A