Canonical Allele Identifier: CA425347306

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238285T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015413T>A , CM000664.2:g.21015413T>A	GRCh38
NC_000002.11:g.21238285T>A , CM000664.1:g.21238285T>A	GRCh37
NC_000002.10:g.21091790T>A	NCBI36
NG_011793.1:g.33661A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2771A>T	ENSP00000501110.2:n.*2771A>T
ENST00000673882.2:c.*2560A>T	ENSP00000501253.2:n.*2560A>T
ENST00000673739.1:c.3179A>T	ENSP00000501110.1:n.3179A>T
ENST00000673882.1:c.2968A>T	ENSP00000501253.1:n.2968A>T
ENST00000233242.5:c.3465A>T MANE Select	ENSP00000233242.1:p.Thr1155=
ENST00000616098.4:c.3465A>T	ENSP00000477990.1:p.Thr1155=
NM_000384.2:c.3465A>T	NP_000375.2:p.Thr1155=
XM_011532809.1:c.3465A>T	XP_011531111.1:p.Thr1155=
NM_000384.3:c.3465A>T MANE Select	NP_000375.3:p.Thr1155=