Canonical Allele Identifier: CA425346283
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21233896G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011024G>C , CM000664.2:g.21011024G>C GRCh38
NC_000002.11:g.21233896G>C , CM000664.1:g.21233896G>C GRCh37
NC_000002.10:g.21087401G>C NCBI36
NG_011793.1:g.38050C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5844C>G MANE Select ENSP00000233242.1:p.Gly1948=
ENST00000616098.4:c.5844C>G ENSP00000477990.1:p.Gly1948=
NM_000384.2:c.5844C>G NP_000375.2:p.Gly1948=
XM_011532809.1:c.5844C>G XP_011531111.1:p.Gly1948=
NM_000384.3:c.5844C>G MANE Select NP_000375.3:p.Gly1948=
Search 100 bp 5'
Search 100 bp 3'