Canonical Allele Identifier: CA2493472552
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1662978945
gnomAD v4: 2-21001650-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21001650T>C , CM000664.2:g.21001650T>C GRCh38
NC_000002.11:g.21224522T>C , CM000664.1:g.21224522T>C GRCh37
NC_000002.10:g.21078027T>C NCBI36
NG_011793.1:g.47424A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.*80A>G MANE Select ENSP00000233242.1:n.*80A>G
ENST00000616098.4:c.13770A>G ENSP00000477990.1:n.13770A>G
NM_000384.2:c.*80A>G NP_000375.2:n.*80A>G
XM_011532809.1:c.5870-2377A>G XP_011531111.1:n.5870-2377A>G
NM_000384.3:c.*80A>G MANE Select NP_000375.3:n.*80A>G
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