Canonical Allele Identifier: CA358027342
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320764G>C , CM000666.2:g.119320764G>C GRCh38
NC_000004.11:g.120241919G>C , CM000666.1:g.120241919G>C GRCh37
NC_000004.10:g.120461367G>C NCBI36
NG_011444.1:g.6398C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.146C>G MANE Select ENSP00000274024.3:p.Thr49Arg
ENST00000274024.3:c.146C>G ENSP00000274024.3:p.Thr49Arg
NM_000134.3:c.146C>G NP_000125.2:p.Thr49Arg
NM_000134.4:c.146C>G MANE Select NP_000125.2:p.Thr49Arg