Canonical Allele Identifier: CA346009073

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238305G>C (hg19) ; chr2:g.21015433G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015433G>C , CM000664.2:g.21015433G>C	GRCh38
NC_000002.11:g.21238305G>C , CM000664.1:g.21238305G>C	GRCh37
NC_000002.10:g.21091810G>C	NCBI36
NG_011793.1:g.33641C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2751C>G	ENSP00000501110.2:n.*2751C>G
ENST00000673882.2:c.*2540C>G	ENSP00000501253.2:n.*2540C>G
ENST00000673739.1:c.3159C>G	ENSP00000501110.1:n.3159C>G
ENST00000673882.1:c.2948C>G	ENSP00000501253.1:n.2948C>G
ENST00000233242.5:c.3445C>G MANE Select	ENSP00000233242.1:p.Gln1149Glu
ENST00000616098.4:c.3445C>G	ENSP00000477990.1:p.Gln1149Glu
NM_000384.2:c.3445C>G	NP_000375.2:p.Gln1149Glu
XM_011532809.1:c.3445C>G	XP_011531111.1:p.Gln1149Glu
NM_000384.3:c.3445C>G MANE Select	NP_000375.3:p.Gln1149Glu