Canonical Allele Identifier: CA2671895033
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320559A>C , CM000666.2:g.119320559A>C GRCh38
NC_000004.11:g.120241714A>C , CM000666.1:g.120241714A>C GRCh37
NC_000004.10:g.120461162A>C NCBI36
NG_011444.1:g.6603T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+111T>G MANE Select ENSP00000274024.3:n.240+111T>G
ENST00000274024.3:c.240+111T>G ENSP00000274024.3:n.240+111T>G
NM_000134.3:c.240+111T>G NP_000125.2:n.240+111T>G
NM_000134.4:c.240+111T>G MANE Select NP_000125.2:n.240+111T>G