Canonical Allele Identifier: CA345969515
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663006024

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21002347A>G , CM000664.2:g.21002347A>G GRCh38
NC_000002.11:g.21225219A>G , CM000664.1:g.21225219A>G GRCh37
NC_000002.10:g.21078724A>G NCBI36
NG_011793.1:g.46727T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.13075T>C MANE Select ENSP00000233242.1:p.Phe4359Leu
ENST00000616098.4:c.13073T>C ENSP00000477990.1:n.13073T>C
NM_000384.2:c.13075T>C NP_000375.2:p.Phe4359Leu
XM_011532809.1:c.5870-3074T>C XP_011531111.1:n.5870-3074T>C
NM_000384.3:c.13075T>C MANE Select NP_000375.3:p.Phe4359Leu