Canonical Allele Identifier: CA2817737856

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026470dup , CM000683.2:g.33026470dup	GRCh38
NC_000021.8:g.34398778dup , CM000683.1:g.34398778dup	GRCh37
NC_000021.7:g.33320648dup	NCBI36
NG_011834.1:g.5540dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-62-331dup MANE Select	ENSP00000371794.3:n.-62-331dup
ENST00000333337.3:c.-393dup	ENSP00000331040.3:n.-393dup
ENST00000382357.3:c.-62-331dup	ENSP00000371794.3:n.-62-331dup
ENST00000430860.1:c.-63+210dup	ENSP00000391183.1:n.-63+210dup
NM_005806.3:c.-62-331dup	NP_005797.1:n.-62-331dup
XM_005260908.1:c.-63+210dup	XP_005260965.1:n.-63+210dup
NM_005806.4:c.-62-331dup MANE Select	NP_005797.1:n.-62-331dup