Canonical Allele Identifier: CA786086672
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1300751132
MyVariant Identifiers: chr4:g.120241615_120241616del (hg19) chr4:g.119320460_119320461del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320461_119320462del , CM000666.2:g.119320461_119320462del GRCh38
NC_000004.11:g.120241616_120241617del , CM000666.1:g.120241616_120241617del GRCh37
NC_000004.10:g.120461064_120461065del NCBI36
NG_011444.1:g.6701_6702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+209_240+210del MANE Select ENSP00000274024.3:n.240+209_240+210del
ENST00000274024.3:c.240+209_240+210del ENSP00000274024.3:n.240+209_240+210del
NM_000134.3:c.240+209_240+210del NP_000125.2:n.240+209_240+210del
NM_000134.4:c.240+209_240+210del MANE Select NP_000125.2:n.240+209_240+210del
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