Canonical Allele Identifier: CA2737611197

Gene: OLIG2

Linked Data

• dbSNP Id: rs2123266085

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026202del , CM000683.2:g.33026202del	GRCh38
NC_000021.8:g.34398510del , CM000683.1:g.34398510del	GRCh37
NC_000021.7:g.33320380del	NCBI36
NG_011834.1:g.5272del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-63+176del MANE Select	ENSP00000371794.3:n.-63+176del
ENST00000333337.3:c.-661del	ENSP00000331040.3:n.-661del
ENST00000382357.3:c.-63+176del	ENSP00000371794.3:n.-63+176del
ENST00000430860.1:c.-121del	ENSP00000391183.1:n.-121del
NM_005806.3:c.-63+176del	NP_005797.1:n.-63+176del
XM_005260908.1:c.-121del	XP_005260965.1:n.-121del
NM_005806.4:c.-63+176del MANE Select	NP_005797.1:n.-63+176del