Canonical Allele Identifier: CA425343878
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21230179T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007307T>A , CM000664.2:g.21007307T>A GRCh38
NC_000002.11:g.21230179T>A , CM000664.1:g.21230179T>A GRCh37
NC_000002.10:g.21083684T>A NCBI36
NG_011793.1:g.41767A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9561A>T MANE Select ENSP00000233242.1:p.Thr3187=
ENST00000616098.4:c.9561A>T ENSP00000477990.1:p.Thr3187=
NM_000384.2:c.9561A>T NP_000375.2:p.Thr3187=
XM_011532809.1:c.5869+3426A>T XP_011531111.1:n.5869+3426A>T
NM_000384.3:c.9561A>T MANE Select NP_000375.3:p.Thr3187=
Search 100 bp 5'
Search 100 bp 3'