Canonical Allele Identifier: CA2386486285

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026280C= , CM000683.2:g.33026280C=	GRCh38
NC_000021.8:g.34398588C= , CM000683.1:g.34398588C=	GRCh37
NC_000021.7:g.33320458C=	NCBI36
NG_011834.1:g.5350C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-63+254C= MANE Select	ENSP00000371794.3:n.-63+254C=
ENST00000333337.3:c.-583C=	ENSP00000331040.3:n.-583C=
ENST00000382357.3:c.-63+254C=	ENSP00000371794.3:n.-63+254C=
ENST00000430860.1:c.-63+20C=	ENSP00000391183.1:n.-63+20C=
NM_005806.3:c.-63+254C=	NP_005797.1:n.-63+254C=
XM_005260908.1:c.-63+20C=	XP_005260965.1:n.-63+20C=
NM_005806.4:c.-63+254C= MANE Select	NP_005797.1:n.-63+254C=