Canonical Allele Identifier: CA2671895029
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320557T>G , CM000666.2:g.119320557T>G GRCh38
NC_000004.11:g.120241712T>G , CM000666.1:g.120241712T>G GRCh37
NC_000004.10:g.120461160T>G NCBI36
NG_011444.1:g.6605A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+113A>C MANE Select ENSP00000274024.3:n.240+113A>C
ENST00000274024.3:c.240+113A>C ENSP00000274024.3:n.240+113A>C
NM_000134.3:c.240+113A>C NP_000125.2:n.240+113A>C
NM_000134.4:c.240+113A>C MANE Select NP_000125.2:n.240+113A>C