Canonical Allele Identifier: CA916487992
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1572778804
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006584_21006585insCA , CM000664.2:g.21006584_21006585insCA GRCh38
NC_000002.11:g.21229456_21229457insCA , CM000664.1:g.21229456_21229457insCA GRCh37
NC_000002.10:g.21082961_21082962insCA NCBI36
NG_011793.1:g.42489_42490insTG

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.10283_10284insTG MANE Select ENSP00000233242.1:p.Thr3429AlafsTer9
ENST00000616098.4:c.10283_10284insTG ENSP00000477990.1:p.Thr3429AlafsTer9
NM_000384.2:c.10283_10284insTG NP_000375.2:p.Thr3429AlafsTer9
XM_011532809.1:c.5869+4148_5869+4149insTG XP_011531111.1:n.5869+4148_5869+4149insTG...
NM_000384.3:c.10283_10284insTG MANE Select NP_000375.3:p.Thr3429AlafsTer9
Search 100 bp 5'
Search 100 bp 3'