Canonical Allele Identifier: CA2493489434
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1664053664
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21038280A>C , CM000664.2:g.21038280A>C GRCh38
NC_000002.11:g.21261152A>C , CM000664.1:g.21261152A>C GRCh37
NC_000002.10:g.21114657A>C NCBI36
NG_011793.1:g.10794T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.384-1025T>G ENSP00000501110.2:n.384-1025T>G
ENST00000673882.2:c.384-1025T>G ENSP00000501253.2:n.384-1025T>G
ENST00000673739.1:c.252-1025T>G ENSP00000501110.1:n.252-1025T>G
ENST00000673882.1:c.252-1025T>G ENSP00000501253.1:n.252-1025T>G
ENST00000233242.5:c.384-169T>G MANE Select ENSP00000233242.1:n.384-169T>G
ENST00000399256.4:c.384-169T>G ENSP00000382200.4:n.384-169T>G
ENST00000616098.4:c.384-169T>G ENSP00000477990.1:n.384-169T>G
NM_000384.2:c.384-169T>G NP_000375.2:n.384-169T>G
XM_011532809.1:c.384-169T>G XP_011531111.1:n.384-169T>G
NM_000384.3:c.384-169T>G MANE Select NP_000375.3:n.384-169T>G
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