Canonical Allele Identifier: CA425137951

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21251249C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028377C>G , CM000664.2:g.21028377C>G	GRCh38
NC_000002.11:g.21251249C>G , CM000664.1:g.21251249C>G	GRCh37
NC_000002.10:g.21104754C>G	NCBI36
NG_011793.1:g.20697G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1085G>C	ENSP00000501110.2:n.*1085G>C
ENST00000673882.2:c.*1085G>C	ENSP00000501253.2:n.*1085G>C
ENST00000673739.1:c.1493G>C	ENSP00000501110.1:n.1493G>C
ENST00000673882.1:c.1493G>C	ENSP00000501253.1:n.1493G>C
ENST00000233242.5:c.1779G>C MANE Select	ENSP00000233242.1:p.Val593=
ENST00000399256.4:c.1779G>C	ENSP00000382200.4:p.Val593=
ENST00000616098.4:c.1779G>C	ENSP00000477990.1:p.Val593=
NM_000384.2:c.1779G>C	NP_000375.2:p.Val593=
XM_011532809.1:c.1779G>C	XP_011531111.1:p.Val593=
NM_000384.3:c.1779G>C MANE Select	NP_000375.3:p.Val593=