Canonical Allele Identifier: CA346007658
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21236163A>T (hg19) chr2:g.21013291A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21013291A>T , CM000664.2:g.21013291A>T GRCh38
NC_000002.11:g.21236163A>T , CM000664.1:g.21236163A>T GRCh37
NC_000002.10:g.21089668A>T NCBI36
NG_011793.1:g.35783T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*3391T>A ENSP00000501110.2:n.*3391T>A
ENST00000673739.1:c.3799T>A ENSP00000501110.1:n.3799T>A
ENST00000233242.5:c.4085T>A MANE Select ENSP00000233242.1:p.Val1362Asp
ENST00000616098.4:c.4085T>A ENSP00000477990.1:p.Val1362Asp
NM_000384.2:c.4085T>A NP_000375.2:p.Val1362Asp
XM_011532809.1:c.4085T>A XP_011531111.1:p.Val1362Asp
NM_000384.3:c.4085T>A MANE Select NP_000375.3:p.Val1362Asp
Search 100 bp 5'
Search 100 bp 3'