Canonical Allele Identifier: CA346003829

Gene: APOB

Linked Data

• COSMIC: COSM4090889
• MyVariant Identifiers: chr2:g.21233884A>T (hg19) ; chr2:g.21011012A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011012A>T , CM000664.2:g.21011012A>T	GRCh38
NC_000002.11:g.21233884A>T , CM000664.1:g.21233884A>T	GRCh37
NC_000002.10:g.21087389A>T	NCBI36
NG_011793.1:g.38062T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5856T>A MANE Select	ENSP00000233242.1:p.His1952Gln
ENST00000616098.4:c.5856T>A	ENSP00000477990.1:p.His1952Gln
NM_000384.2:c.5856T>A	NP_000375.2:p.His1952Gln
XM_011532809.1:c.5856T>A	XP_011531111.1:p.His1952Gln
NM_000384.3:c.5856T>A MANE Select	NP_000375.3:p.His1952Gln