Canonical Allele Identifier: CA425346278

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21233893G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011021G>T , CM000664.2:g.21011021G>T	GRCh38
NC_000002.11:g.21233893G>T , CM000664.1:g.21233893G>T	GRCh37
NC_000002.10:g.21087398G>T	NCBI36
NG_011793.1:g.38053C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5847C>A MANE Select	ENSP00000233242.1:p.Ser1949=
ENST00000616098.4:c.5847C>A	ENSP00000477990.1:p.Ser1949=
NM_000384.2:c.5847C>A	NP_000375.2:p.Ser1949=
XM_011532809.1:c.5847C>A	XP_011531111.1:p.Ser1949=
NM_000384.3:c.5847C>A MANE Select	NP_000375.3:p.Ser1949=