Canonical Allele Identifier: CA11180724
Gene: APOB HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10199768

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21021128G>T , CM000664.2:g.21021128G>T GRCh38
NC_000002.11:g.21244000G>T , CM000664.1:g.21244000G>T GRCh37
NC_000002.10:g.21097505G>T NCBI36
NG_011793.1:g.27946C>A

Transcript Alleles

HGVS Amino-acid change
NM_000384.2:c.2817-1223C>A VV NP_000375.2:p.=
XM_011532809.1:c.2817-1223C>A XP_011531111.1:p.=
ENST00000233242.5:c.2817-1223C>A ENSP00000233242.1:p.=
ENST00000616098.4:n.2817-1223C>A ENSP00000477990.1:p.=