Canonical Allele Identifier: CA2493478789
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21014924T= , CM000664.2:g.21014924T= GRCh38
NC_000002.11:g.21237796T= , CM000664.1:g.21237796T= GRCh37
NC_000002.10:g.21091301T= NCBI36
NG_011793.1:g.34150A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*3002+149A= ENSP00000501110.2:n.*3002+149A=
ENST00000673882.2:c.*2791+149A= ENSP00000501253.2:n.*2791+149A=
ENST00000673739.1:c.3410+149A= ENSP00000501110.1:n.3410+149A=
ENST00000673882.1:c.3199+149A= ENSP00000501253.1:n.3199+149A=
ENST00000233242.5:c.3696+149A= MANE Select ENSP00000233242.1:n.3696+149A=
ENST00000616098.4:c.3696+149A= ENSP00000477990.1:n.3696+149A=
NM_000384.2:c.3696+149A= NP_000375.2:n.3696+149A=
XM_011532809.1:c.3696+149A= XP_011531111.1:n.3696+149A=
NM_000384.3:c.3696+149A= MANE Select NP_000375.3:n.3696+149A=
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