Canonical Allele Identifier: CA2749100018

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028322C>T , CM000664.2:g.21028322C>T	GRCh38
NC_000002.11:g.21251194C>T , CM000664.1:g.21251194C>T	GRCh37
NC_000002.10:g.21104699C>T	NCBI36
NG_011793.1:g.20752G>A

Transcript Alleles

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