Canonical Allele Identifier: CA358026984

Gene: FABP2

Linked Data

• dbSNP Id: rs1755652963
• MyVariant Identifiers: chr4:g.120241868C>G (hg19) ; chr4:g.119320713C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320713C>G , CM000666.2:g.119320713C>G	GRCh38
NC_000004.11:g.120241868C>G , CM000666.1:g.120241868C>G	GRCh37
NC_000004.10:g.120461316C>G	NCBI36
NG_011444.1:g.6449G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.197G>C MANE Select	ENSP00000274024.3:p.Gly66Ala
ENST00000274024.3:c.197G>C	ENSP00000274024.3:p.Gly66Ala
NM_000134.3:c.197G>C	NP_000125.2:p.Gly66Ala
NM_000134.4:c.197G>C MANE Select	NP_000125.2:p.Gly66Ala