Canonical Allele Identifier: CA1028210223

Gene: APOB

Linked Data

• dbSNP Id: rs1664044616
• gnomAD v3: 2-21037902-CT-C
• gnomAD v4: 2-21037902-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037903del , CM000664.2:g.21037903del	GRCh38
NC_000002.11:g.21260775del , CM000664.1:g.21260775del	GRCh37
NC_000002.10:g.21114280del	NCBI36
NG_011793.1:g.11171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-648del	ENSP00000501110.2:n.384-648del
ENST00000673882.2:c.384-648del	ENSP00000501253.2:n.384-648del
ENST00000673739.1:c.252-648del	ENSP00000501110.1:n.252-648del
ENST00000673882.1:c.252-648del	ENSP00000501253.1:n.252-648del
ENST00000233242.5:c.537+55del MANE Select	ENSP00000233242.1:n.537+55del
ENST00000399256.4:c.537+55del	ENSP00000382200.4:n.537+55del
ENST00000616098.4:c.537+55del	ENSP00000477990.1:n.537+55del
NM_000384.2:c.537+55del	NP_000375.2:n.537+55del
XM_011532809.1:c.537+55del	XP_011531111.1:n.537+55del
NM_000384.3:c.537+55del MANE Select	NP_000375.3:n.537+55del