Canonical Allele Identifier: CA2671895126
Gene: FABP2 HGNC NCBI

Linked Data

gnomAD v4: 4-119320763-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320764del , CM000666.2:g.119320764del GRCh38
NC_000004.11:g.120241919del , CM000666.1:g.120241919del GRCh37
NC_000004.10:g.120461367del NCBI36
NG_011444.1:g.6398del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.146del MANE Select ENSP00000274024.3:p.Thr49LysfsTer25
ENST00000274024.3:c.146del ENSP00000274024.3:p.Thr49LysfsTer25
NM_000134.3:c.146del NP_000125.2:p.Thr49LysfsTer25
NM_000134.4:c.146del MANE Select NP_000125.2:p.Thr49LysfsTer25
Search 100 bp 5'
Search 100 bp 3'