Canonical Allele Identifier: CA346003795

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21233868T>A (hg19) ; chr2:g.21010996T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21010996T>A , CM000664.2:g.21010996T>A	GRCh38
NC_000002.11:g.21233868T>A , CM000664.1:g.21233868T>A	GRCh37
NC_000002.10:g.21087373T>A	NCBI36
NG_011793.1:g.38078A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5872A>T MANE Select	ENSP00000233242.1:p.Lys1958Ter
ENST00000616098.4:c.5872A>T	ENSP00000477990.1:p.Lys1958Ter
NM_000384.2:c.5872A>T	NP_000375.2:p.Lys1958Ter
XM_011532809.1:c.5864+8A>T	XP_011531111.1:n.5864+8A>T
NM_000384.3:c.5872A>T MANE Select	NP_000375.3:p.Lys1958Ter