Canonical Allele Identifier: CA358026972
Gene: FABP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320711C>A , CM000666.2:g.119320711C>A GRCh38
NC_000004.11:g.120241866C>A , CM000666.1:g.120241866C>A GRCh37
NC_000004.10:g.120461314C>A NCBI36
NG_011444.1:g.6451G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.199G>T MANE Select ENSP00000274024.3:p.Val67Phe
ENST00000274024.3:c.199G>T ENSP00000274024.3:p.Val67Phe
NM_000134.3:c.199G>T NP_000125.2:p.Val67Phe
NM_000134.4:c.199G>T MANE Select NP_000125.2:p.Val67Phe