Canonical Allele Identifier: CA345970613

Gene: APOB

Linked Data

• dbSNP Id: rs1663022355
• MyVariant Identifiers: chr2:g.21225567A>G (hg19) ; chr2:g.21002695A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21002695A>G , CM000664.2:g.21002695A>G	GRCh38
NC_000002.11:g.21225567A>G , CM000664.1:g.21225567A>G	GRCh37
NC_000002.10:g.21079072A>G	NCBI36
NG_011793.1:g.46379T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.12727T>C MANE Select	ENSP00000233242.1:p.Phe4243Leu
ENST00000616098.4:c.12727T>C	ENSP00000477990.1:p.Phe4243Leu
NM_000384.2:c.12727T>C	NP_000375.2:p.Phe4243Leu
XM_011532809.1:c.5870-3422T>C	XP_011531111.1:n.5870-3422T>C
NM_000384.3:c.12727T>C MANE Select	NP_000375.3:p.Phe4243Leu