Canonical Allele Identifier: CA2671895083
Gene: FABP2 HGNC NCBI

Linked Data

gnomAD v4: 4-119320631-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320631A>C , CM000666.2:g.119320631A>C GRCh38
NC_000004.11:g.120241786A>C , CM000666.1:g.120241786A>C GRCh37
NC_000004.10:g.120461234A>C NCBI36
NG_011444.1:g.6531T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+39T>G MANE Select ENSP00000274024.3:n.240+39T>G
ENST00000274024.3:c.240+39T>G ENSP00000274024.3:n.240+39T>G
NM_000134.3:c.240+39T>G NP_000125.2:n.240+39T>G
NM_000134.4:c.240+39T>G MANE Select NP_000125.2:n.240+39T>G
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