Canonical Allele Identifier: CA425345436
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21232978A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010106A>G , CM000664.2:g.21010106A>G GRCh38
NC_000002.11:g.21232978A>G , CM000664.1:g.21232978A>G GRCh37
NC_000002.10:g.21086483A>G NCBI36
NG_011793.1:g.38968T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.6762T>C MANE Select ENSP00000233242.1:p.Thr2254=
ENST00000616098.4:c.6762T>C ENSP00000477990.1:p.Thr2254=
NM_000384.2:c.6762T>C NP_000375.2:p.Thr2254=
XM_011532809.1:c.5869+627T>C XP_011531111.1:n.5869+627T>C
NM_000384.3:c.6762T>C MANE Select NP_000375.3:p.Thr2254=
Search 100 bp 5'
Search 100 bp 3'