Canonical Allele Identifier: CA425136171

Gene: APOB

Linked Data

• ClinVar Variation Id: 2451323
• ClinVar RCV Id: RCV003182339
• gnomAD v4: 2-21013299-G-A
• MyVariant Identifiers: chr2:g.21236171G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21013299G>A , CM000664.2:g.21013299G>A	GRCh38
NC_000002.11:g.21236171G>A , CM000664.1:g.21236171G>A	GRCh37
NC_000002.10:g.21089676G>A	NCBI36
NG_011793.1:g.35775C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*3383C>T	ENSP00000501110.2:n.*3383C>T
ENST00000673882.2:c.*3172C>T	ENSP00000501253.2:n.*3172C>T
ENST00000673739.1:c.3791C>T	ENSP00000501110.1:n.3791C>T
ENST00000673882.1:c.3580C>T	ENSP00000501253.1:n.3580C>T
ENST00000233242.5:c.4077C>T MANE Select	ENSP00000233242.1:p.Ser1359=
ENST00000616098.4:c.4077C>T	ENSP00000477990.1:p.Ser1359=
NM_000384.2:c.4077C>T	NP_000375.2:p.Ser1359=
XM_011532809.1:c.4077C>T	XP_011531111.1:p.Ser1359=
NM_000384.3:c.4077C>T MANE Select	NP_000375.3:p.Ser1359=