Canonical Allele Identifier: CA2493476951
Gene: APOB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011007_21011010delinsAGAT , CM000664.2:g.21011007_21011010delinsAGAT GRCh38
NC_000002.11:g.21233879_21233882delinsAGAT , CM000664.1:g.21233879_21233882delinsAGAT GRCh37
NC_000002.10:g.21087384_21087387delinsAGAT NCBI36
NG_011793.1:g.38064_38067delinsATCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5858_5861delinsATCT MANE Select ENSP00000233242.1:p.His1953=
ENST00000616098.4:c.5858_5861delinsATCT ENSP00000477990.1:p.His1953=
NM_000384.2:c.5858_5861delinsATCT NP_000375.2:p.His1953=
XM_011532809.1:c.5858_5861delinsATCT XP_011531111.1:p.His1953=
NM_000384.3:c.5858_5861delinsATCT MANE Select NP_000375.3:p.His1953=
Search 100 bp 5'
Search 100 bp 3'