Canonical Allele Identifier: CA425121072

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21260890G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038018G>A , CM000664.2:g.21038018G>A	GRCh38
NC_000002.11:g.21260890G>A , CM000664.1:g.21260890G>A	GRCh37
NC_000002.10:g.21114395G>A	NCBI36
NG_011793.1:g.11056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-763C>T	ENSP00000501110.2:n.384-763C>T
ENST00000673882.2:c.384-763C>T	ENSP00000501253.2:n.384-763C>T
ENST00000673739.1:c.252-763C>T	ENSP00000501110.1:n.252-763C>T
ENST00000673882.1:c.252-763C>T	ENSP00000501253.1:n.252-763C>T
ENST00000233242.5:c.477C>T MANE Select	ENSP00000233242.1:p.Gly159=
ENST00000399256.4:c.477C>T	ENSP00000382200.4:p.Gly159=
ENST00000616098.4:c.477C>T	ENSP00000477990.1:p.Gly159=
NM_000384.2:c.477C>T	NP_000375.2:p.Gly159=
XM_011532809.1:c.477C>T	XP_011531111.1:p.Gly159=
NM_000384.3:c.477C>T MANE Select	NP_000375.3:p.Gly159=