Canonical Allele Identifier: CA2493478760
Gene: APOB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21014858T= , CM000664.2:g.21014858T= GRCh38
NC_000002.11:g.21237730T= , CM000664.1:g.21237730T= GRCh37
NC_000002.10:g.21091235T= NCBI36
NG_011793.1:g.34216A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*3002+215A= ENSP00000501110.2:n.*3002+215A=
ENST00000673882.2:c.*2791+215A= ENSP00000501253.2:n.*2791+215A=
ENST00000673739.1:c.3410+215A= ENSP00000501110.1:n.3410+215A=
ENST00000673882.1:c.3199+215A= ENSP00000501253.1:n.3199+215A=
ENST00000233242.5:c.3696+215A= MANE Select ENSP00000233242.1:n.3696+215A=
ENST00000616098.4:c.3696+215A= ENSP00000477990.1:n.3696+215A=
NM_000384.2:c.3696+215A= NP_000375.2:n.3696+215A=
XM_011532809.1:c.3696+215A= XP_011531111.1:n.3696+215A=
NM_000384.3:c.3696+215A= MANE Select NP_000375.3:n.3696+215A=