Canonical Allele Identifier: CA748767341

Gene: OLIG2

Linked Data

• dbSNP Id: rs1268149004
• gnomAD v3: 21-33026406-A-G
• gnomAD v4: 21-33026406-A-G
• MyVariant Identifiers: chr21:g.34398714A>G (hg19) ; chr21:g.33026406A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026406A>G , CM000683.2:g.33026406A>G	GRCh38
NC_000021.8:g.34398714A>G , CM000683.1:g.34398714A>G	GRCh37
NC_000021.7:g.33320584A>G	NCBI36
NG_011834.1:g.5476A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-63+380A>G MANE Select	ENSP00000371794.3:n.-63+380A>G
ENST00000333337.3:c.-457A>G	ENSP00000331040.3:n.-457A>G
ENST00000382357.3:c.-63+380A>G	ENSP00000371794.3:n.-63+380A>G
ENST00000430860.1:c.-63+146A>G	ENSP00000391183.1:n.-63+146A>G
NM_005806.3:c.-63+380A>G	NP_005797.1:n.-63+380A>G
XM_005260908.1:c.-63+146A>G	XP_005260965.1:n.-63+146A>G
NM_005806.4:c.-63+380A>G MANE Select	NP_005797.1:n.-63+380A>G