Canonical Allele Identifier: CA060888
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334184
dbSNP Id: rs6752026

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21038062G>A , CM000664.2:g.21038062G>A GRCh38
NC_000002.11:g.21260934G>A , CM000664.1:g.21260934G>A GRCh37
NC_000002.10:g.21114439G>A NCBI36
NG_011793.1:g.11012C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000673739.1:n.252-807C>T ENSP00000501110.1:p.=
ENST00000673882.1:n.252-807C>T ENSP00000501253.1:p.=
ENST00000233242.5:c.433C>T MANE Select ENSP00000233242.1:p.Pro145Ser
ENST00000399256.4:c.433C>T ENSP00000382200.4:p.Pro145Ser
ENST00000616098.4:n.433C>T ENSP00000477990.1:p.Pro145Ser
NM_000384.2:c.433C>T NP_000375.2:p.Pro145Ser
XM_011532809.1:c.433C>T XP_011531111.1:p.Pro145Ser
NM_000384.3:c.433C>T MANE Select NP_000375.3:p.Pro145Ser