Canonical Allele Identifier: CA2654283892
Gene: OLIG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026527_33026543del , CM000683.2:g.33026527_33026543del GRCh38
NC_000021.8:g.34398835_34398851del , CM000683.1:g.34398835_34398851del GRCh37
NC_000021.7:g.33320705_33320721del NCBI36
NG_011834.1:g.5597_5613del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-62-274_-62-258del MANE Select ENSP00000371794.3:n.-62-274_-62-258del
ENST00000333337.3:c.-336_-320del ENSP00000331040.3:n.-336_-320del
ENST00000382357.3:c.-62-274_-62-258del ENSP00000371794.3:n.-62-274_-62-258del
ENST00000430860.1:c.-63+267_-62-258del ENSP00000391183.1:n.-63+267_-62-258del
NM_005806.3:c.-62-274_-62-258del NP_005797.1:n.-62-274_-62-258del
XM_005260908.1:c.-63+267_-62-258del XP_005260965.1:n.-63+267_-62-258del
NM_005806.4:c.-62-274_-62-258del MANE Select NP_005797.1:n.-62-274_-62-258del