Canonical Allele Identifier: CA1488878511
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320670_119320672delinsCCT , CM000666.2:g.119320670_119320672delinsCCT GRCh38
NC_000004.11:g.120241825_120241827delinsCCT , CM000666.1:g.120241825_120241827delinsCCT GRCh37
NC_000004.10:g.120461273_120461275delinsCCT NCBI36
NG_011444.1:g.6490_6492delinsAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.238_240delinsAGG MANE Select ENSP00000274024.3:p.Arg80=
ENST00000274024.3:c.238_240delinsAGG ENSP00000274024.3:p.Arg80=
NM_000134.3:c.238_240delinsAGG NP_000125.2:p.Arg80=
NM_000134.4:c.238_240delinsAGG MANE Select NP_000125.2:p.Arg80=