Canonical Allele Identifier: CA358026886

Gene: FABP2

Linked Data

• MyVariant Identifiers: chr4:g.120241854A>G (hg19) ; chr4:g.119320699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320699A>G , CM000666.2:g.119320699A>G	GRCh38
NC_000004.11:g.120241854A>G , CM000666.1:g.120241854A>G	GRCh37
NC_000004.10:g.120461302A>G	NCBI36
NG_011444.1:g.6463T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.211T>C MANE Select	ENSP00000274024.3:p.Tyr71His
ENST00000274024.3:c.211T>C	ENSP00000274024.3:p.Tyr71His
NM_000134.3:c.211T>C	NP_000125.2:p.Tyr71His
NM_000134.4:c.211T>C MANE Select	NP_000125.2:p.Tyr71His