Canonical Allele Identifier: CA2654283825
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs2123266463
gnomAD v4: 21-33026465-CG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026470del , CM000683.2:g.33026470del GRCh38
NC_000021.8:g.34398778del , CM000683.1:g.34398778del GRCh37
NC_000021.7:g.33320648del NCBI36
NG_011834.1:g.5540del

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-62-331del MANE Select ENSP00000371794.3:n.-62-331del
ENST00000333337.3:c.-393del ENSP00000331040.3:n.-393del
ENST00000382357.3:c.-62-331del ENSP00000371794.3:n.-62-331del
ENST00000430860.1:c.-63+210del ENSP00000391183.1:n.-63+210del
NM_005806.3:c.-62-331del NP_005797.1:n.-62-331del
XM_005260908.1:c.-63+210del XP_005260965.1:n.-63+210del
NM_005806.4:c.-62-331del MANE Select NP_005797.1:n.-62-331del
Search 100 bp 5'
Search 100 bp 3'