Canonical Allele Identifier: CA2576687092
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21037893G>T , CM000664.2:g.21037893G>T GRCh38
NC_000002.11:g.21260765G>T , CM000664.1:g.21260765G>T GRCh37
NC_000002.10:g.21114270G>T NCBI36
NG_011793.1:g.11181C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.384-638C>A ENSP00000501110.2:n.384-638C>A
ENST00000673882.2:c.384-638C>A ENSP00000501253.2:n.384-638C>A
ENST00000673739.1:c.252-638C>A ENSP00000501110.1:n.252-638C>A
ENST00000673882.1:c.252-638C>A ENSP00000501253.1:n.252-638C>A
ENST00000233242.5:c.537+65C>A MANE Select ENSP00000233242.1:n.537+65C>A
ENST00000399256.4:c.537+65C>A ENSP00000382200.4:n.537+65C>A
ENST00000616098.4:c.537+65C>A ENSP00000477990.1:n.537+65C>A
NM_000384.2:c.537+65C>A NP_000375.2:n.537+65C>A
XM_011532809.1:c.537+65C>A XP_011531111.1:n.537+65C>A
NM_000384.3:c.537+65C>A MANE Select NP_000375.3:n.537+65C>A
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