Canonical Allele Identifier: CA2576687087

Gene: APOB

Linked Data

• gnomAD v4: 2-21037868-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21037868C>T , CM000664.2:g.21037868C>T	GRCh38
NC_000002.11:g.21260740C>T , CM000664.1:g.21260740C>T	GRCh37
NC_000002.10:g.21114245C>T	NCBI36
NG_011793.1:g.11206G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.384-613G>A	ENSP00000501110.2:n.384-613G>A
ENST00000673882.2:c.384-613G>A	ENSP00000501253.2:n.384-613G>A
ENST00000673739.1:c.252-613G>A	ENSP00000501110.1:n.252-613G>A
ENST00000673882.1:c.252-613G>A	ENSP00000501253.1:n.252-613G>A
ENST00000233242.5:c.537+90G>A MANE Select	ENSP00000233242.1:n.537+90G>A
ENST00000399256.4:c.537+90G>A	ENSP00000382200.4:n.537+90G>A
ENST00000616098.4:c.537+90G>A	ENSP00000477990.1:n.537+90G>A
NM_000384.2:c.537+90G>A	NP_000375.2:n.537+90G>A
XM_011532809.1:c.537+90G>A	XP_011531111.1:n.537+90G>A
NM_000384.3:c.537+90G>A MANE Select	NP_000375.3:n.537+90G>A