Canonical Allele Identifier: CA2493478971
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015280A= , CM000664.2:g.21015280A= GRCh38
NC_000002.11:g.21238152A= , CM000664.1:g.21238152A= GRCh37
NC_000002.10:g.21091657A= NCBI36
NG_011793.1:g.33794T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2815-20T= ENSP00000501110.2:n.*2815-20T=
ENST00000673882.2:c.*2604-20T= ENSP00000501253.2:n.*2604-20T=
ENST00000673739.1:c.3223-20T= ENSP00000501110.1:n.3223-20T=
ENST00000673882.1:c.3012-20T= ENSP00000501253.1:n.3012-20T=
ENST00000233242.5:c.3509-20T= MANE Select ENSP00000233242.1:n.3509-20T=
ENST00000616098.4:c.3509-20T= ENSP00000477990.1:n.3509-20T=
NM_000384.2:c.3509-20T= NP_000375.2:n.3509-20T=
XM_011532809.1:c.3509-20T= XP_011531111.1:n.3509-20T=
NM_000384.3:c.3509-20T= MANE Select NP_000375.3:n.3509-20T=
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