Canonical Allele Identifier: CA2493489267
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21037947T= , CM000664.2:g.21037947T= GRCh38
NC_000002.11:g.21260819T= , CM000664.1:g.21260819T= GRCh37
NC_000002.10:g.21114324T= NCBI36
NG_011793.1:g.11127A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.384-692A= ENSP00000501110.2:n.384-692A=
ENST00000673882.2:c.384-692A= ENSP00000501253.2:n.384-692A=
ENST00000673739.1:c.252-692A= ENSP00000501110.1:n.252-692A=
ENST00000673882.1:c.252-692A= ENSP00000501253.1:n.252-692A=
ENST00000233242.5:c.537+11A= MANE Select ENSP00000233242.1:n.537+11A=
ENST00000399256.4:c.537+11A= ENSP00000382200.4:n.537+11A=
ENST00000616098.4:c.537+11A= ENSP00000477990.1:n.537+11A=
NM_000384.2:c.537+11A= NP_000375.2:n.537+11A=
XM_011532809.1:c.537+11A= XP_011531111.1:n.537+11A=
NM_000384.3:c.537+11A= MANE Select NP_000375.3:n.537+11A=
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