Canonical Allele Identifier: CA1021917166
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981071455

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026378_33026389del , CM000683.2:g.33026378_33026389del GRCh38
NC_000021.8:g.34398686_34398697del , CM000683.1:g.34398686_34398697del GRCh37
NC_000021.7:g.33320556_33320567del NCBI36
NG_011834.1:g.5448_5459del

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+352_-63+363del MANE Select ENSP00000371794.3:n.-63+352_-63+363del
ENST00000333337.3:c.-485_-474del ENSP00000331040.3:n.-485_-474del
ENST00000382357.3:c.-63+352_-63+363del ENSP00000371794.3:n.-63+352_-63+363del
ENST00000430860.1:c.-63+118_-63+129del ENSP00000391183.1:n.-63+118_-63+129del
NM_005806.3:c.-63+352_-63+363del NP_005797.1:n.-63+352_-63+363del
XM_005260908.1:c.-63+118_-63+129del XP_005260965.1:n.-63+118_-63+129del
NM_005806.4:c.-63+352_-63+363del MANE Select NP_005797.1:n.-63+352_-63+363del