Canonical Allele Identifier: CA2578177590
Gene: FABP2 HGNC NCBI

Linked Data

gnomAD v4: 4-119320648-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320648T>C , CM000666.2:g.119320648T>C GRCh38
NC_000004.11:g.120241803T>C , CM000666.1:g.120241803T>C GRCh37
NC_000004.10:g.120461251T>C NCBI36
NG_011444.1:g.6514A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+22A>G MANE Select ENSP00000274024.3:n.240+22A>G
ENST00000274024.3:c.240+22A>G ENSP00000274024.3:n.240+22A>G
NM_000134.3:c.240+22A>G NP_000125.2:n.240+22A>G
NM_000134.4:c.240+22A>G MANE Select NP_000125.2:n.240+22A>G
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