Canonical Allele Identifier: CA346014486

Gene: APOB

Linked Data

• dbSNP Id: rs774406602
• COSMIC: COSM3426055
• MyVariant Identifiers: chr2:g.21251273C>A (hg19) ; chr2:g.21028401C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028401C>A , CM000664.2:g.21028401C>A	GRCh38
NC_000002.11:g.21251273C>A , CM000664.1:g.21251273C>A	GRCh37
NC_000002.10:g.21104778C>A	NCBI36
NG_011793.1:g.20673G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*1061G>T	ENSP00000501110.2:n.*1061G>T
ENST00000673882.2:c.*1061G>T	ENSP00000501253.2:n.*1061G>T
ENST00000673739.1:c.1469G>T	ENSP00000501110.1:n.1469G>T
ENST00000673882.1:c.1469G>T	ENSP00000501253.1:n.1469G>T
ENST00000233242.5:c.1755G>T MANE Select	ENSP00000233242.1:p.Gln585His
ENST00000399256.4:c.1755G>T	ENSP00000382200.4:p.Gln585His
ENST00000616098.4:c.1755G>T	ENSP00000477990.1:p.Gln585His
NM_000384.2:c.1755G>T	NP_000375.2:p.Gln585His
XM_011532809.1:c.1755G>T	XP_011531111.1:p.Gln585His
NM_000384.3:c.1755G>T MANE Select	NP_000375.3:p.Gln585His