Canonical Allele Identifier: CA425347287

Gene: APOB

Linked Data

• dbSNP Id: rs1461980758
• gnomAD v2: 2-21238258-C-T
• gnomAD v4: 2-21015386-C-T
• MyVariant Identifiers: chr2:g.21238258C>T (hg19) ; chr2:g.21015386C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015386C>T , CM000664.2:g.21015386C>T	GRCh38
NC_000002.11:g.21238258C>T , CM000664.1:g.21238258C>T	GRCh37
NC_000002.10:g.21091763C>T	NCBI36
NG_011793.1:g.33688G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2798G>A	ENSP00000501110.2:n.*2798G>A
ENST00000673882.2:c.*2587G>A	ENSP00000501253.2:n.*2587G>A
ENST00000673739.1:c.3206G>A	ENSP00000501110.1:n.3206G>A
ENST00000673882.1:c.2995G>A	ENSP00000501253.1:n.2995G>A
ENST00000233242.5:c.3492G>A MANE Select	ENSP00000233242.1:p.Arg1164=
ENST00000616098.4:c.3492G>A	ENSP00000477990.1:p.Arg1164=
NM_000384.2:c.3492G>A	NP_000375.2:p.Arg1164=
XM_011532809.1:c.3492G>A	XP_011531111.1:p.Arg1164=
NM_000384.3:c.3492G>A MANE Select	NP_000375.3:p.Arg1164=