Canonical Allele Identifier: CA358027596
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241942A>C (hg19) chr4:g.119320787A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320787A>C , CM000666.2:g.119320787A>C GRCh38
NC_000004.11:g.120241942A>C , CM000666.1:g.120241942A>C GRCh37
NC_000004.10:g.120461390A>C NCBI36
NG_011444.1:g.6375T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.123T>G MANE Select ENSP00000274024.3:p.Ile41Met
ENST00000274024.3:c.123T>G ENSP00000274024.3:p.Ile41Met
NM_000134.3:c.123T>G NP_000125.2:p.Ile41Met
NM_000134.4:c.123T>G MANE Select NP_000125.2:p.Ile41Met
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