Canonical Allele Identifier: CA522177699

Gene: FABP3

Linked Data

• dbSNP Id: rs1175383768
• gnomAD v2: 1-31845777-C-T
• MyVariant Identifiers: chr1:g.31845777C>T (hg19) ; chr1:g.31372930C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31372930C>T , CM000663.2:g.31372930C>T	GRCh38
NC_000001.10:g.31845777C>T , CM000663.1:g.31845777C>T	GRCh37
NC_000001.9:g.31618364C>T	NCBI36
NG_047049.1:g.5354G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373713.7:c.73+12G>A MANE Select	ENSP00000362817.2:n.73+12G>A
ENST00000373713.6:c.73+12G>A	ENSP00000362817.2:n.73+12G>A
ENST00000482018.1:c.73+12G>A	ENSP00000473982.1:n.73+12G>A
ENST00000498148.5:c.73+12G>A	ENSP00000474078.1:n.73+12G>A
NM_004102.3:c.73+12G>A	NP_004093.1:n.73+12G>A
XM_011541007.1:c.73+12G>A	XP_011539309.1:n.73+12G>A
NM_001320996.1:c.73+12G>A	NP_001307925.1:n.73+12G>A
NM_004102.4:c.73+12G>A	NP_004093.1:n.73+12G>A
XM_011541007.3:c.73+12G>A	XP_011539309.1:n.73+12G>A
NM_004102.5:c.73+12G>A MANE Select	NP_004093.1:n.73+12G>A
NM_001320996.2:c.73+12G>A	NP_001307925.1:n.73+12G>A