Canonical Allele Identifier: CA339578466

Gene: FABP3

Linked Data

• dbSNP Id: rs191192801
• gnomAD v2: 1-31845835-C-G
• gnomAD v4: 1-31372988-C-G
• MyVariant Identifiers: chr1:g.31845835C>G (hg19) ; chr1:g.31372988C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31372988C>G , CM000663.2:g.31372988C>G	GRCh38
NC_000001.10:g.31845835C>G , CM000663.1:g.31845835C>G	GRCh37
NC_000001.9:g.31618422C>G	NCBI36
NG_047049.1:g.5296G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.27G>C MANE Select	ENSP00000362817.2:p.Trp9Cys
ENST00000373713.6:c.27G>C	ENSP00000362817.2:p.Trp9Cys
ENST00000482018.1:c.27G>C	ENSP00000473982.1:p.Trp9Cys
ENST00000498148.5:c.27G>C	ENSP00000474078.1:p.Trp9Cys
NM_004102.3:c.27G>C	NP_004093.1:p.Trp9Cys
XM_011541007.1:c.27G>C	XP_011539309.1:p.Trp9Cys
NM_001320996.1:c.27G>C	NP_001307925.1:p.Trp9Cys
NM_004102.4:c.27G>C	NP_004093.1:p.Trp9Cys
XM_011541007.3:c.27G>C	XP_011539309.1:p.Trp9Cys
NM_004102.5:c.27G>C MANE Select	NP_004093.1:p.Trp9Cys
NM_001320996.2:c.27G>C	NP_001307925.1:p.Trp9Cys