Canonical Allele Identifier: CA358027855

Gene: FABP2

Linked Data

• MyVariant Identifiers: chr4:g.120241978C>G (hg19) ; chr4:g.119320823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320823C>G , CM000666.2:g.119320823C>G	GRCh38
NC_000004.11:g.120241978C>G , CM000666.1:g.120241978C>G	GRCh37
NC_000004.10:g.120461426C>G	NCBI36
NG_011444.1:g.6339G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.87G>C MANE Select	ENSP00000274024.3:p.Arg29Ser
ENST00000274024.3:c.87G>C	ENSP00000274024.3:p.Arg29Ser
NM_000134.3:c.87G>C	NP_000125.2:p.Arg29Ser
NM_000134.4:c.87G>C MANE Select	NP_000125.2:p.Arg29Ser