Canonical Allele Identifier: CA1488878485
Gene: FABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320603C= , CM000666.2:g.119320603C= GRCh38
NC_000004.11:g.120241758C= , CM000666.1:g.120241758C= GRCh37
NC_000004.10:g.120461206C= NCBI36
NG_011444.1:g.6559G=

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+67G= MANE Select ENSP00000274024.3:n.240+67G=
ENST00000274024.3:c.240+67G= ENSP00000274024.3:n.240+67G=
NM_000134.3:c.240+67G= NP_000125.2:n.240+67G=
NM_000134.4:c.240+67G= MANE Select NP_000125.2:n.240+67G=