Canonical Allele Identifier: CA913089799
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21234203_21234205del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011335_21011337del , CM000664.2:g.21011335_21011337del GRCh38
NC_000002.11:g.21234207_21234209del , CM000664.1:g.21234207_21234209del GRCh37
NC_000002.10:g.21087712_21087714del NCBI36
NG_011793.1:g.37741_37743del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5535_5537del MANE Select ENSP00000233242.1:p.Ala1846del
ENST00000616098.4:c.5535_5537del ENSP00000477990.1:p.Ala1846del
NM_000384.2:c.5535_5537del NP_000375.2:p.Ala1846del
XM_011532809.1:c.5535_5537del XP_011531111.1:p.Ala1846del
NM_000384.3:c.5535_5537del MANE Select NP_000375.3:p.Ala1846del
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