Canonical Allele Identifier: CA2493478980
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015304C= , CM000664.2:g.21015304C= GRCh38
NC_000002.11:g.21238176C= , CM000664.1:g.21238176C= GRCh37
NC_000002.10:g.21091681C= NCBI36
NG_011793.1:g.33770G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2815-44G= ENSP00000501110.2:n.*2815-44G=
ENST00000673882.2:c.*2604-44G= ENSP00000501253.2:n.*2604-44G=
ENST00000673739.1:c.3223-44G= ENSP00000501110.1:n.3223-44G=
ENST00000673882.1:c.3012-44G= ENSP00000501253.1:n.3012-44G=
ENST00000233242.5:c.3509-44G= MANE Select ENSP00000233242.1:n.3509-44G=
ENST00000616098.4:c.3509-44G= ENSP00000477990.1:n.3509-44G=
NM_000384.2:c.3509-44G= NP_000375.2:n.3509-44G=
XM_011532809.1:c.3509-44G= XP_011531111.1:n.3509-44G=
NM_000384.3:c.3509-44G= MANE Select NP_000375.3:n.3509-44G=
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