Canonical Allele Identifier: CA2658048665

Gene: APOB

Linked Data

• gnomAD v4: 2-21028297-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028297T>C , CM000664.2:g.21028297T>C	GRCh38
NC_000002.11:g.21251169T>C , CM000664.1:g.21251169T>C	GRCh37
NC_000002.10:g.21104674T>C	NCBI36
NG_011793.1:g.20777A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*1135+30A>G	ENSP00000501110.2:n.*1135+30A>G
ENST00000673882.2:c.*1135+30A>G	ENSP00000501253.2:n.*1135+30A>G
ENST00000673739.1:c.1543+30A>G	ENSP00000501110.1:n.1543+30A>G
ENST00000673882.1:c.1543+30A>G	ENSP00000501253.1:n.1543+30A>G
ENST00000233242.5:c.1829+30A>G MANE Select	ENSP00000233242.1:n.1829+30A>G
ENST00000399256.4:c.1829+30A>G	ENSP00000382200.4:n.1829+30A>G
ENST00000616098.4:c.1829+30A>G	ENSP00000477990.1:n.1829+30A>G
NM_000384.2:c.1829+30A>G	NP_000375.2:n.1829+30A>G
XM_011532809.1:c.1829+30A>G	XP_011531111.1:n.1829+30A>G
NM_000384.3:c.1829+30A>G MANE Select	NP_000375.3:n.1829+30A>G