Canonical Allele Identifier: CA730577

Gene: FABP3

Linked Data

• dbSNP Id: rs767698076
• ExAC: 1:31845816 T / C
• gnomAD v2: 1-31845816-T-C
• gnomAD v3: 1-31372969-T-C
• gnomAD v4: 1-31372969-T-C
• MyVariant Identifiers: chr1:g.31845816T>C (hg19) ; chr1:g.31372969T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31372969T>C , CM000663.2:g.31372969T>C	GRCh38
NC_000001.10:g.31845816T>C , CM000663.1:g.31845816T>C	GRCh37
NC_000001.9:g.31618403T>C	NCBI36
NG_047049.1:g.5315A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.46A>G MANE Select	ENSP00000362817.2:p.Asn16Asp
ENST00000373713.6:c.46A>G	ENSP00000362817.2:p.Asn16Asp
ENST00000482018.1:c.46A>G	ENSP00000473982.1:p.Asn16Asp
ENST00000498148.5:c.46A>G	ENSP00000474078.1:p.Asn16Asp
NM_004102.3:c.46A>G	NP_004093.1:p.Asn16Asp
XM_011541007.1:c.46A>G	XP_011539309.1:p.Asn16Asp
NM_001320996.1:c.46A>G	NP_001307925.1:p.Asn16Asp
NM_004102.4:c.46A>G	NP_004093.1:p.Asn16Asp
XM_011541007.3:c.46A>G	XP_011539309.1:p.Asn16Asp
NM_004102.5:c.46A>G MANE Select	NP_004093.1:p.Asn16Asp
NM_001320996.2:c.46A>G	NP_001307925.1:p.Asn16Asp