Canonical Allele Identifier: CA2493472578
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1662979954

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001713A>C , CM000664.2:g.21001713A>C GRCh38
NC_000002.11:g.21224585A>C , CM000664.1:g.21224585A>C GRCh37
NC_000002.10:g.21078090A>C NCBI36
NG_011793.1:g.47361T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*17T>G MANE Select ENSP00000233242.1:n.*17T>G
ENST00000616098.4:c.13707T>G ENSP00000477990.1:n.13707T>G
NM_000384.2:c.*17T>G NP_000375.2:n.*17T>G
XM_011532809.1:c.5870-2440T>G XP_011531111.1:n.5870-2440T>G
NM_000384.3:c.*17T>G MANE Select NP_000375.3:n.*17T>G