Canonical Allele Identifier: CA2493476972
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011037_21011039delinsTGA , CM000664.2:g.21011037_21011039delinsTGA GRCh38
NC_000002.11:g.21233909_21233911delinsTGA , CM000664.1:g.21233909_21233911delinsTGA GRCh37
NC_000002.10:g.21087414_21087416delinsTGA NCBI36
NG_011793.1:g.38035_38037delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5829_5831delinsTCA MANE Select ENSP00000233242.1:p.Ser1943=
ENST00000616098.4:c.5829_5831delinsTCA ENSP00000477990.1:p.Ser1943=
NM_000384.2:c.5829_5831delinsTCA NP_000375.2:p.Ser1943=
XM_011532809.1:c.5829_5831delinsTCA XP_011531111.1:p.Ser1943=
NM_000384.3:c.5829_5831delinsTCA MANE Select NP_000375.3:p.Ser1943=
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