Canonical Allele Identifier: CA425343372
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21229453T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006581T>G , CM000664.2:g.21006581T>G GRCh38
NC_000002.11:g.21229453T>G , CM000664.1:g.21229453T>G GRCh37
NC_000002.10:g.21082958T>G NCBI36
NG_011793.1:g.42493A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.10287A>C MANE Select ENSP00000233242.1:p.Thr3429=
ENST00000616098.4:c.10287A>C ENSP00000477990.1:p.Thr3429=
NM_000384.2:c.10287A>C NP_000375.2:p.Thr3429=
XM_011532809.1:c.5869+4152A>C XP_011531111.1:n.5869+4152A>C
NM_000384.3:c.10287A>C MANE Select NP_000375.3:p.Thr3429=
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