Canonical Allele Identifier: CA3059768
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs755247535

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320665C>T , CM000666.2:g.119320665C>T GRCh38
NC_000004.11:g.120241820C>T , CM000666.1:g.120241820C>T GRCh37
NC_000004.10:g.120461268C>T NCBI36
NG_011444.1:g.6497G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+5G>A MANE Select ENSP00000274024.3:n.240+5G>A
ENST00000274024.3:c.240+5G>A ENSP00000274024.3:n.240+5G>A
NM_000134.3:c.240+5G>A NP_000125.2:n.240+5G>A
NM_000134.4:c.240+5G>A MANE Select NP_000125.2:n.240+5G>A