Canonical Allele Identifier: CA345988732

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21229935C>T (hg19) ; chr2:g.21007063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21007063C>T , CM000664.2:g.21007063C>T	GRCh38
NC_000002.11:g.21229935C>T , CM000664.1:g.21229935C>T	GRCh37
NC_000002.10:g.21083440C>T	NCBI36
NG_011793.1:g.42011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.9805G>A MANE Select	ENSP00000233242.1:p.Ala3269Thr
ENST00000616098.4:c.9805G>A	ENSP00000477990.1:p.Ala3269Thr
NM_000384.2:c.9805G>A	NP_000375.2:p.Ala3269Thr
XM_011532809.1:c.5869+3670G>A	XP_011531111.1:n.5869+3670G>A
NM_000384.3:c.9805G>A MANE Select	NP_000375.3:p.Ala3269Thr