Canonical Allele Identifier: CA1488878586
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755656593
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320839_119320840insATGCCATAGTCTC , CM000666.2:g.119320839_119320840insATGCCATAGTCTC GRCh38
NC_000004.11:g.120241994_120241995insATGCCATAGTCTC , CM000666.1:g.120241994_120241995insATGCCATAGTCTC GRCh37
NC_000004.10:g.120461442_120461443insATGCCATAGTCTC NCBI36
NG_011444.1:g.6322_6323insGAGACTATGGCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.70_71insGAGACTATGGCAT MANE Select ENSP00000274024.3:p.Val24GlyfsTer6
ENST00000274024.3:c.70_71insGAGACTATGGCAT ENSP00000274024.3:p.Val24GlyfsTer6
NM_000134.3:c.70_71insGAGACTATGGCAT NP_000125.2:p.Val24GlyfsTer6
NM_000134.4:c.70_71insGAGACTATGGCAT MANE Select NP_000125.2:p.Val24GlyfsTer6
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