Canonical Allele Identifier: CA3059769
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs374808911

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320666T>C , CM000666.2:g.119320666T>C GRCh38
NC_000004.11:g.120241821T>C , CM000666.1:g.120241821T>C GRCh37
NC_000004.10:g.120461269T>C NCBI36
NG_011444.1:g.6496A>G

Transcript Alleles

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