Canonical Allele Identifier: CA425347282

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238252T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015380T>C , CM000664.2:g.21015380T>C	GRCh38
NC_000002.11:g.21238252T>C , CM000664.1:g.21238252T>C	GRCh37
NC_000002.10:g.21091757T>C	NCBI36
NG_011793.1:g.33694A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2804A>G	ENSP00000501110.2:n.*2804A>G
ENST00000673882.2:c.*2593A>G	ENSP00000501253.2:n.*2593A>G
ENST00000673739.1:c.3212A>G	ENSP00000501110.1:n.3212A>G
ENST00000673882.1:c.3001A>G	ENSP00000501253.1:n.3001A>G
ENST00000233242.5:c.3498A>G MANE Select	ENSP00000233242.1:p.Ala1166=
ENST00000616098.4:c.3498A>G	ENSP00000477990.1:p.Ala1166=
NM_000384.2:c.3498A>G	NP_000375.2:p.Ala1166=
XM_011532809.1:c.3498A>G	XP_011531111.1:p.Ala1166=
NM_000384.3:c.3498A>G MANE Select	NP_000375.3:p.Ala1166=