Canonical Allele Identifier: CA2573051852
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs2103357685
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010964_21010967dup , CM000664.2:g.21010964_21010967dup GRCh38
NC_000002.11:g.21233836_21233839dup , CM000664.1:g.21233836_21233839dup GRCh37
NC_000002.10:g.21087341_21087344dup NCBI36
NG_011793.1:g.38110_38113dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5904_5907dup MANE Select ENSP00000233242.1:p.Ala1970GlnfsTer8
ENST00000616098.4:c.5904_5907dup ENSP00000477990.1:p.Ala1970GlnfsTer8
NM_000384.2:c.5904_5907dup NP_000375.2:p.Ala1970GlnfsTer8
XM_011532809.1:c.5864+40_5864+43dup XP_011531111.1:n.5864+40_5864+43dup
NM_000384.3:c.5904_5907dup MANE Select NP_000375.3:p.Ala1970GlnfsTer8
Search 100 bp 5'
Search 100 bp 3'