Canonical Allele Identifier: CA1067271661
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755649417

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320556G>A , CM000666.2:g.119320556G>A GRCh38
NC_000004.11:g.120241711G>A , CM000666.1:g.120241711G>A GRCh37
NC_000004.10:g.120461159G>A NCBI36
NG_011444.1:g.6606C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+114C>T MANE Select ENSP00000274024.3:n.240+114C>T
ENST00000274024.3:c.240+114C>T ENSP00000274024.3:n.240+114C>T
NM_000134.3:c.240+114C>T NP_000125.2:n.240+114C>T
NM_000134.4:c.240+114C>T MANE Select NP_000125.2:n.240+114C>T