Canonical Allele Identifier: CA345986965
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006631T>G , CM000664.2:g.21006631T>G GRCh38
NC_000002.11:g.21229503T>G , CM000664.1:g.21229503T>G GRCh37
NC_000002.10:g.21083008T>G NCBI36
NG_011793.1:g.42443A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.10237A>C MANE Select ENSP00000233242.1:p.Thr3413Pro
ENST00000616098.4:c.10237A>C ENSP00000477990.1:p.Thr3413Pro
NM_000384.2:c.10237A>C NP_000375.2:p.Thr3413Pro
XM_011532809.1:c.5869+4102A>C XP_011531111.1:n.5869+4102A>C
NM_000384.3:c.10237A>C MANE Select NP_000375.3:p.Thr3413Pro