Canonical Allele Identifier: CA764121090

Gene: APOB

Linked Data

• dbSNP Id: rs1254931127
• MyVariant Identifiers: chr2:g.21243926C>T (hg19) ; chr2:g.21021054C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21021054C>T , CM000664.2:g.21021054C>T	GRCh38
NC_000002.11:g.21243926C>T , CM000664.1:g.21243926C>T	GRCh37
NC_000002.10:g.21097431C>T	NCBI36
NG_011793.1:g.28020G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*2123-1149G>A	ENSP00000501110.2:n.*2123-1149G>A
ENST00000673882.2:c.*2123-1149G>A	ENSP00000501253.2:n.*2123-1149G>A
ENST00000673739.1:c.2531-1149G>A	ENSP00000501110.1:n.2531-1149G>A
ENST00000673882.1:c.2531-1149G>A	ENSP00000501253.1:n.2531-1149G>A
ENST00000233242.5:c.2817-1149G>A MANE Select	ENSP00000233242.1:n.2817-1149G>A
ENST00000616098.4:c.2817-1149G>A	ENSP00000477990.1:n.2817-1149G>A
NM_000384.2:c.2817-1149G>A	NP_000375.2:n.2817-1149G>A
XM_011532809.1:c.2817-1149G>A	XP_011531111.1:n.2817-1149G>A
NM_000384.3:c.2817-1149G>A MANE Select	NP_000375.3:n.2817-1149G>A