Canonical Allele Identifier: CA2671895013
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320549T>C , CM000666.2:g.119320549T>C GRCh38
NC_000004.11:g.120241704T>C , CM000666.1:g.120241704T>C GRCh37
NC_000004.10:g.120461152T>C NCBI36
NG_011444.1:g.6613A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+121A>G MANE Select ENSP00000274024.3:n.240+121A>G
ENST00000274024.3:c.240+121A>G ENSP00000274024.3:n.240+121A>G
NM_000134.3:c.240+121A>G NP_000125.2:n.240+121A>G
NM_000134.4:c.240+121A>G MANE Select NP_000125.2:n.240+121A>G