Canonical Allele Identifier: CA2386486246

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026186A= , CM000683.2:g.33026186A=	GRCh38
NC_000021.8:g.34398494A= , CM000683.1:g.34398494A=	GRCh37
NC_000021.7:g.33320364A=	NCBI36
NG_011834.1:g.5256A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+160A= MANE Select	ENSP00000371794.3:n.-63+160A=
ENST00000333337.3:c.-677A=	ENSP00000331040.3:n.-677A=
ENST00000382357.3:c.-63+160A=	ENSP00000371794.3:n.-63+160A=
ENST00000430860.1:c.-137A=	ENSP00000391183.1:n.-137A=
NM_005806.3:c.-63+160A=	NP_005797.1:n.-63+160A=
XM_005260908.1:c.-137A=	XP_005260965.1:n.-137A=
NM_005806.4:c.-63+160A= MANE Select	NP_005797.1:n.-63+160A=