Canonical Allele Identifier: CA2654283889

Gene: OLIG2

Linked Data

• gnomAD v4: 21-33026520-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026520_33026521insG , CM000683.2:g.33026520_33026521insG	GRCh38
NC_000021.8:g.34398828_34398829insG , CM000683.1:g.34398828_34398829insG	GRCh37
NC_000021.7:g.33320698_33320699insG	NCBI36
NG_011834.1:g.5590_5591insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-62-281_-62-280insG MANE Select	ENSP00000371794.3:n.-62-281_-62-280insG
ENST00000333337.3:c.-343_-342insG	ENSP00000331040.3:n.-343_-342insG
ENST00000382357.3:c.-62-281_-62-280insG	ENSP00000371794.3:n.-62-281_-62-280insG
ENST00000430860.1:c.-63+260_-63+261insG	ENSP00000391183.1:n.-63+260_-63+261insG
NM_005806.3:c.-62-281_-62-280insG	NP_005797.1:n.-62-281_-62-280insG
XM_005260908.1:c.-63+260_-63+261insG	XP_005260965.1:n.-63+260_-63+261insG
NM_005806.4:c.-62-281_-62-280insG MANE Select	NP_005797.1:n.-62-281_-62-280insG