Canonical Allele Identifier: CA440890869
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241912T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320757T>C , CM000666.2:g.119320757T>C GRCh38
NC_000004.11:g.120241912T>C , CM000666.1:g.120241912T>C GRCh37
NC_000004.10:g.120461360T>C NCBI36
NG_011444.1:g.6405A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.153A>G MANE Select ENSP00000274024.3:p.Lys51=
ENST00000274024.3:c.153A>G ENSP00000274024.3:p.Lys51=
NM_000134.3:c.153A>G NP_000125.2:p.Lys51=
NM_000134.4:c.153A>G MANE Select NP_000125.2:p.Lys51=