Canonical Allele Identifier: CA346003801
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs868467341

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010998C>G , CM000664.2:g.21010998C>G GRCh38
NC_000002.11:g.21233870C>G , CM000664.1:g.21233870C>G GRCh37
NC_000002.10:g.21087375C>G NCBI36
NG_011793.1:g.38076G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5870G>C MANE Select ENSP00000233242.1:p.Arg1957Thr
ENST00000616098.4:c.5870G>C ENSP00000477990.1:p.Arg1957Thr
NM_000384.2:c.5870G>C NP_000375.2:p.Arg1957Thr
XM_011532809.1:c.5864+6G>C XP_011531111.1:n.5864+6G>C
NM_000384.3:c.5870G>C MANE Select NP_000375.3:p.Arg1957Thr