Canonical Allele Identifier: CA2671894974
Gene: FABP2 HGNC NCBI

Linked Data

gnomAD v4: 4-119320518-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320518G>T , CM000666.2:g.119320518G>T GRCh38
NC_000004.11:g.120241673G>T , CM000666.1:g.120241673G>T GRCh37
NC_000004.10:g.120461121G>T NCBI36
NG_011444.1:g.6644C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+152C>A MANE Select ENSP00000274024.3:n.240+152C>A
ENST00000274024.3:c.240+152C>A ENSP00000274024.3:n.240+152C>A
NM_000134.3:c.240+152C>A NP_000125.2:n.240+152C>A
NM_000134.4:c.240+152C>A MANE Select NP_000125.2:n.240+152C>A
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