Canonical Allele Identifier: CA764121117

Gene: APOB

Linked Data

• dbSNP Id: rs1398011622
• MyVariant Identifiers: chr2:g.21243960del (hg19) ; chr2:g.21021088del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21021088del , CM000664.2:g.21021088del	GRCh38
NC_000002.11:g.21243960del , CM000664.1:g.21243960del	GRCh37
NC_000002.10:g.21097465del	NCBI36
NG_011793.1:g.27986del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2123-1183del	ENSP00000501110.2:n.*2123-1183del
ENST00000673882.2:c.*2123-1183del	ENSP00000501253.2:n.*2123-1183del
ENST00000673739.1:c.2531-1183del	ENSP00000501110.1:n.2531-1183del
ENST00000673882.1:c.2531-1183del	ENSP00000501253.1:n.2531-1183del
ENST00000233242.5:c.2817-1183del MANE Select	ENSP00000233242.1:n.2817-1183del
ENST00000616098.4:c.2817-1183del	ENSP00000477990.1:n.2817-1183del
NM_000384.2:c.2817-1183del	NP_000375.2:n.2817-1183del
XM_011532809.1:c.2817-1183del	XP_011531111.1:n.2817-1183del
NM_000384.3:c.2817-1183del MANE Select	NP_000375.3:n.2817-1183del