Canonical Allele Identifier: CA346008927
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21238133C>T (hg19) chr2:g.21015261C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21015261C>T , CM000664.2:g.21015261C>T GRCh38
NC_000002.11:g.21238133C>T , CM000664.1:g.21238133C>T GRCh37
NC_000002.10:g.21091638C>T NCBI36
NG_011793.1:g.33813G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673739.2:c.*2815-1G>A ENSP00000501110.2:n.*2815-1G>A
ENST00000673882.2:c.*2604-1G>A ENSP00000501253.2:n.*2604-1G>A
ENST00000673739.1:c.3223-1G>A ENSP00000501110.1:n.3223-1G>A
ENST00000673882.1:c.3012-1G>A ENSP00000501253.1:n.3012-1G>A
ENST00000233242.5:c.3509-1G>A MANE Select ENSP00000233242.1:n.3509-1G>A
ENST00000616098.4:c.3509-1G>A ENSP00000477990.1:n.3509-1G>A
NM_000384.2:c.3509-1G>A NP_000375.2:n.3509-1G>A
XM_011532809.1:c.3509-1G>A XP_011531111.1:n.3509-1G>A
NM_000384.3:c.3509-1G>A MANE Select NP_000375.3:n.3509-1G>A
Search 100 bp 5'
Search 100 bp 3'