Canonical Allele Identifier: CA345997171
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009436C>G , CM000664.2:g.21009436C>G GRCh38
NC_000002.11:g.21232308C>G , CM000664.1:g.21232308C>G GRCh37
NC_000002.10:g.21085813C>G NCBI36
NG_011793.1:g.39638G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7432G>C MANE Select ENSP00000233242.1:p.Ala2478Pro
ENST00000616098.4:c.7432G>C ENSP00000477990.1:p.Ala2478Pro
NM_000384.2:c.7432G>C NP_000375.2:p.Ala2478Pro
XM_011532809.1:c.5869+1297G>C XP_011531111.1:n.5869+1297G>C
NM_000384.3:c.7432G>C MANE Select NP_000375.3:p.Ala2478Pro