Canonical Allele Identifier: CA345967032
Gene: APOB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001819T>C , CM000664.2:g.21001819T>C GRCh38
NC_000002.11:g.21224691T>C , CM000664.1:g.21224691T>C GRCh37
NC_000002.10:g.21078196T>C NCBI36
NG_011793.1:g.47255A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13603A>G MANE Select ENSP00000233242.1:p.Ile4535Val
ENST00000616098.4:c.13601A>G ENSP00000477990.1:n.13601A>G
NM_000384.2:c.13603A>G NP_000375.2:p.Ile4535Val
XM_011532809.1:c.5870-2546A>G XP_011531111.1:n.5870-2546A>G
NM_000384.3:c.13603A>G MANE Select NP_000375.3:p.Ile4535Val