Canonical Allele Identifier: CA425343917
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21230191C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007319C>T , CM000664.2:g.21007319C>T GRCh38
NC_000002.11:g.21230191C>T , CM000664.1:g.21230191C>T GRCh37
NC_000002.10:g.21083696C>T NCBI36
NG_011793.1:g.41755G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9549G>A MANE Select ENSP00000233242.1:p.Arg3183=
ENST00000616098.4:c.9549G>A ENSP00000477990.1:p.Arg3183=
NM_000384.2:c.9549G>A NP_000375.2:p.Arg3183=
XM_011532809.1:c.5869+3414G>A XP_011531111.1:n.5869+3414G>A
NM_000384.3:c.9549G>A MANE Select NP_000375.3:p.Arg3183=