Canonical Allele Identifier: CA345997200
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009450G>C , CM000664.2:g.21009450G>C GRCh38
NC_000002.11:g.21232322G>C , CM000664.1:g.21232322G>C GRCh37
NC_000002.10:g.21085827G>C NCBI36
NG_011793.1:g.39624C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7418C>G MANE Select ENSP00000233242.1:p.Thr2473Ser
ENST00000616098.4:c.7418C>G ENSP00000477990.1:p.Thr2473Ser
NM_000384.2:c.7418C>G NP_000375.2:p.Thr2473Ser
XM_011532809.1:c.5869+1283C>G XP_011531111.1:n.5869+1283C>G
NM_000384.3:c.7418C>G MANE Select NP_000375.3:p.Thr2473Ser