Canonical Allele Identifier: CA2386486317
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026348G= , CM000683.2:g.33026348G= GRCh38
NC_000021.8:g.34398656G= , CM000683.1:g.34398656G= GRCh37
NC_000021.7:g.33320526G= NCBI36
NG_011834.1:g.5418G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+322G= MANE Select ENSP00000371794.3:n.-63+322G=
ENST00000333337.3:c.-515G= ENSP00000331040.3:n.-515G=
ENST00000382357.3:c.-63+322G= ENSP00000371794.3:n.-63+322G=
ENST00000430860.1:c.-63+88G= ENSP00000391183.1:n.-63+88G=
NM_005806.3:c.-63+322G= NP_005797.1:n.-63+322G=
XM_005260908.1:c.-63+88G= XP_005260965.1:n.-63+88G=
NM_005806.4:c.-63+322G= MANE Select NP_005797.1:n.-63+322G=