Canonical Allele Identifier: CA320091818

Gene: OLIG2

Linked Data

• dbSNP Id: rs560389836
• gnomAD v2: 21-34398860-A-G
• gnomAD v3: 21-33026552-A-G
• gnomAD v4: 21-33026552-A-G
• MyVariant Identifiers: chr21:g.34398860A>G (hg19) ; chr21:g.33026552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026552A>G , CM000683.2:g.33026552A>G	GRCh38
NC_000021.8:g.34398860A>G , CM000683.1:g.34398860A>G	GRCh37
NC_000021.7:g.33320730A>G	NCBI36
NG_011834.1:g.5622A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-62-249A>G MANE Select	ENSP00000371794.3:n.-62-249A>G
ENST00000333337.3:c.-311A>G	ENSP00000331040.3:n.-311A>G
ENST00000382357.3:c.-62-249A>G	ENSP00000371794.3:n.-62-249A>G
ENST00000430860.1:c.-62-249A>G	ENSP00000391183.1:n.-62-249A>G
NM_005806.3:c.-62-249A>G	NP_005797.1:n.-62-249A>G
XM_005260908.1:c.-62-249A>G	XP_005260965.1:n.-62-249A>G
NM_005806.4:c.-62-249A>G MANE Select	NP_005797.1:n.-62-249A>G