Canonical Allele Identifier: CA346014472

Gene: APOB

Linked Data

• gnomAD v4: 2-21028398-A-T
• MyVariant Identifiers: chr2:g.21251270A>T (hg19) ; chr2:g.21028398A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028398A>T , CM000664.2:g.21028398A>T	GRCh38
NC_000002.11:g.21251270A>T , CM000664.1:g.21251270A>T	GRCh37
NC_000002.10:g.21104775A>T	NCBI36
NG_011793.1:g.20676T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*1064T>A	ENSP00000501110.2:n.*1064T>A
ENST00000673882.2:c.*1064T>A	ENSP00000501253.2:n.*1064T>A
ENST00000673739.1:c.1472T>A	ENSP00000501110.1:n.1472T>A
ENST00000673882.1:c.1472T>A	ENSP00000501253.1:n.1472T>A
ENST00000233242.5:c.1758T>A MANE Select	ENSP00000233242.1:p.Asn586Lys
ENST00000399256.4:c.1758T>A	ENSP00000382200.4:p.Asn586Lys
ENST00000616098.4:c.1758T>A	ENSP00000477990.1:p.Asn586Lys
NM_000384.2:c.1758T>A	NP_000375.2:p.Asn586Lys
XM_011532809.1:c.1758T>A	XP_011531111.1:p.Asn586Lys
NM_000384.3:c.1758T>A MANE Select	NP_000375.3:p.Asn586Lys