Canonical Allele Identifier: CA346002684

Gene: APOB

Linked Data

• dbSNP Id: rs1663290888
• MyVariant Identifiers: chr2:g.21233639A>T (hg19) ; chr2:g.21010767A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21010767A>T , CM000664.2:g.21010767A>T	GRCh38
NC_000002.11:g.21233639A>T , CM000664.1:g.21233639A>T	GRCh37
NC_000002.10:g.21087144A>T	NCBI36
NG_011793.1:g.38307T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.6101T>A MANE Select	ENSP00000233242.1:p.Ile2034Asn
ENST00000616098.4:c.6101T>A	ENSP00000477990.1:p.Ile2034Asn
NM_000384.2:c.6101T>A	NP_000375.2:p.Ile2034Asn
XM_011532809.1:c.5865-30T>A	XP_011531111.1:n.5865-30T>A
NM_000384.3:c.6101T>A MANE Select	NP_000375.3:p.Ile2034Asn