Canonical Allele Identifier: CA345969707

Gene: APOB

Linked Data

• dbSNP Id: rs1663006787
• MyVariant Identifiers: chr2:g.21225258T>A (hg19) ; chr2:g.21002386T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21002386T>A , CM000664.2:g.21002386T>A	GRCh38
NC_000002.11:g.21225258T>A , CM000664.1:g.21225258T>A	GRCh37
NC_000002.10:g.21078763T>A	NCBI36
NG_011793.1:g.46688A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.13036A>T MANE Select	ENSP00000233242.1:p.Lys4346Ter
ENST00000616098.4:c.13034A>T	ENSP00000477990.1:p.Ter4345Leu
NM_000384.2:c.13036A>T	NP_000375.2:p.Lys4346Ter
XM_011532809.1:c.5870-3113A>T	XP_011531111.1:n.5870-3113A>T
NM_000384.3:c.13036A>T MANE Select	NP_000375.3:p.Lys4346Ter