Canonical Allele Identifier: CA43502858
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs961029998

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009594T>C , CM000664.2:g.21009594T>C GRCh38
NC_000002.11:g.21232466T>C , CM000664.1:g.21232466T>C GRCh37
NC_000002.10:g.21085971T>C NCBI36
NG_011793.1:g.39480A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7274A>G MANE Select ENSP00000233242.1:p.Lys2425Arg
ENST00000616098.4:c.7274A>G ENSP00000477990.1:p.Lys2425Arg
NM_000384.2:c.7274A>G NP_000375.2:p.Lys2425Arg
XM_011532809.1:c.5869+1139A>G XP_011531111.1:n.5869+1139A>G
NM_000384.3:c.7274A>G MANE Select NP_000375.3:p.Lys2425Arg