Canonical Allele Identifier: CA2658046654

Gene: APOB

Linked Data

• gnomAD v4: 2-21023456-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21023456G>A , CM000664.2:g.21023456G>A	GRCh38
NC_000002.11:g.21246328G>A , CM000664.1:g.21246328G>A	GRCh37
NC_000002.10:g.21099833G>A	NCBI36
NG_011793.1:g.25618C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*1910+69C>T	ENSP00000501110.2:n.*1910+69C>T
ENST00000673882.2:c.*1910+69C>T	ENSP00000501253.2:n.*1910+69C>T
ENST00000673739.1:c.2318+69C>T	ENSP00000501110.1:n.2318+69C>T
ENST00000673882.1:c.2318+69C>T	ENSP00000501253.1:n.2318+69C>T
ENST00000233242.5:c.2604+69C>T MANE Select	ENSP00000233242.1:n.2604+69C>T
ENST00000616098.4:c.2604+69C>T	ENSP00000477990.1:n.2604+69C>T
NM_000384.2:c.2604+69C>T	NP_000375.2:n.2604+69C>T
XM_011532809.1:c.2604+69C>T	XP_011531111.1:n.2604+69C>T
NM_000384.3:c.2604+69C>T MANE Select	NP_000375.3:n.2604+69C>T