Canonical Allele Identifier: CA748767235

Gene: OLIG2

Linked Data

• dbSNP Id: rs1250170384
• MyVariant Identifiers: chr21:g.34398522G>T (hg19) ; chr21:g.33026214G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026214G>T , CM000683.2:g.33026214G>T	GRCh38
NC_000021.8:g.34398522G>T , CM000683.1:g.34398522G>T	GRCh37
NC_000021.7:g.33320392G>T	NCBI36
NG_011834.1:g.5284G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+188G>T MANE Select	ENSP00000371794.3:n.-63+188G>T
ENST00000333337.3:c.-649G>T	ENSP00000331040.3:n.-649G>T
ENST00000382357.3:c.-63+188G>T	ENSP00000371794.3:n.-63+188G>T
ENST00000430860.1:c.-109G>T	ENSP00000391183.1:n.-109G>T
NM_005806.3:c.-63+188G>T	NP_005797.1:n.-63+188G>T
XM_005260908.1:c.-109G>T	XP_005260965.1:n.-109G>T
NM_005806.4:c.-63+188G>T MANE Select	NP_005797.1:n.-63+188G>T