Canonical Allele Identifier: CA2386486334
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026378G= , CM000683.2:g.33026378G= GRCh38
NC_000021.8:g.34398686G= , CM000683.1:g.34398686G= GRCh37
NC_000021.7:g.33320556G= NCBI36
NG_011834.1:g.5448G=

Transcript Alleles

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