Canonical Allele Identifier: CA2386486272
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026254T= , CM000683.2:g.33026254T= GRCh38
NC_000021.8:g.34398562T= , CM000683.1:g.34398562T= GRCh37
NC_000021.7:g.33320432T= NCBI36
NG_011834.1:g.5324T=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+228T= MANE Select ENSP00000371794.3:n.-63+228T=
ENST00000333337.3:c.-609T= ENSP00000331040.3:n.-609T=
ENST00000382357.3:c.-63+228T= ENSP00000371794.3:n.-63+228T=
ENST00000430860.1:c.-69T= ENSP00000391183.1:n.-69T=
NM_005806.3:c.-63+228T= NP_005797.1:n.-63+228T=
XM_005260908.1:c.-69T= XP_005260965.1:n.-69T=
NM_005806.4:c.-63+228T= MANE Select NP_005797.1:n.-63+228T=