Canonical Allele Identifier: CA2386486372
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026446C= , CM000683.2:g.33026446C= GRCh38
NC_000021.8:g.34398754C= , CM000683.1:g.34398754C= GRCh37
NC_000021.7:g.33320624C= NCBI36
NG_011834.1:g.5516C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-62-355C= MANE Select ENSP00000371794.3:n.-62-355C=
ENST00000333337.3:c.-417C= ENSP00000331040.3:n.-417C=
ENST00000382357.3:c.-62-355C= ENSP00000371794.3:n.-62-355C=
ENST00000430860.1:c.-63+186C= ENSP00000391183.1:n.-63+186C=
NM_005806.3:c.-62-355C= NP_005797.1:n.-62-355C=
XM_005260908.1:c.-63+186C= XP_005260965.1:n.-63+186C=
NM_005806.4:c.-62-355C= MANE Select NP_005797.1:n.-62-355C=