Canonical Allele Identifier: CA425346137
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21233401T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010529T>C , CM000664.2:g.21010529T>C GRCh38
NC_000002.11:g.21233401T>C , CM000664.1:g.21233401T>C GRCh37
NC_000002.10:g.21086906T>C NCBI36
NG_011793.1:g.38545A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.6339A>G MANE Select ENSP00000233242.1:p.Ala2113=
ENST00000616098.4:c.6339A>G ENSP00000477990.1:p.Ala2113=
NM_000384.2:c.6339A>G NP_000375.2:p.Ala2113=
XM_011532809.1:c.5869+204A>G XP_011531111.1:n.5869+204A>G
NM_000384.3:c.6339A>G MANE Select NP_000375.3:p.Ala2113=
Search 100 bp 5'
Search 100 bp 3'