Canonical Allele Identifier: CA346008796

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238079T>C (hg19) ; chr2:g.21015207T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015207T>C , CM000664.2:g.21015207T>C	GRCh38
NC_000002.11:g.21238079T>C , CM000664.1:g.21238079T>C	GRCh37
NC_000002.10:g.21091584T>C	NCBI36
NG_011793.1:g.33867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2868A>G	ENSP00000501110.2:n.*2868A>G
ENST00000673882.2:c.*2657A>G	ENSP00000501253.2:n.*2657A>G
ENST00000673739.1:c.3276A>G	ENSP00000501110.1:n.3276A>G
ENST00000673882.1:c.3065A>G	ENSP00000501253.1:n.3065A>G
ENST00000233242.5:c.3562A>G MANE Select	ENSP00000233242.1:p.Lys1188Glu
ENST00000616098.4:c.3562A>G	ENSP00000477990.1:p.Lys1188Glu
NM_000384.2:c.3562A>G	NP_000375.2:p.Lys1188Glu
XM_011532809.1:c.3562A>G	XP_011531111.1:p.Lys1188Glu
NM_000384.3:c.3562A>G MANE Select	NP_000375.3:p.Lys1188Glu