Canonical Allele Identifier: CA346003852
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1558564705
gnomAD v4: 2-21011023-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011023A>G , CM000664.2:g.21011023A>G GRCh38
NC_000002.11:g.21233895A>G , CM000664.1:g.21233895A>G GRCh37
NC_000002.10:g.21087400A>G NCBI36
NG_011793.1:g.38051T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5845T>C MANE Select ENSP00000233242.1:p.Ser1949Pro
ENST00000616098.4:c.5845T>C ENSP00000477990.1:p.Ser1949Pro
NM_000384.2:c.5845T>C NP_000375.2:p.Ser1949Pro
XM_011532809.1:c.5845T>C XP_011531111.1:p.Ser1949Pro
NM_000384.3:c.5845T>C MANE Select NP_000375.3:p.Ser1949Pro