Canonical Allele Identifier: CA346008887

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238118C>T (hg19) ; chr2:g.21015246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015246C>T , CM000664.2:g.21015246C>T	GRCh38
NC_000002.11:g.21238118C>T , CM000664.1:g.21238118C>T	GRCh37
NC_000002.10:g.21091623C>T	NCBI36
NG_011793.1:g.33828G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2829G>A	ENSP00000501110.2:n.*2829G>A
ENST00000673882.2:c.*2618G>A	ENSP00000501253.2:n.*2618G>A
ENST00000673739.1:c.3237G>A	ENSP00000501110.1:n.3237G>A
ENST00000673882.1:c.3026G>A	ENSP00000501253.1:n.3026G>A
ENST00000233242.5:c.3523G>A MANE Select	ENSP00000233242.1:p.Glu1175Lys
ENST00000616098.4:c.3523G>A	ENSP00000477990.1:p.Glu1175Lys
NM_000384.2:c.3523G>A	NP_000375.2:p.Glu1175Lys
XM_011532809.1:c.3523G>A	XP_011531111.1:p.Glu1175Lys
NM_000384.3:c.3523G>A MANE Select	NP_000375.3:p.Glu1175Lys