Canonical Allele Identifier: CA320091793

Gene: OLIG2

Linked Data

• dbSNP Id: rs576380596
• gnomAD v2: 21-34398579-C-T
• gnomAD v3: 21-33026271-C-T
• gnomAD v4: 21-33026271-C-T
• MyVariant Identifiers: chr21:g.34398579C>T (hg19) ; chr21:g.33026271C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026271C>T , CM000683.2:g.33026271C>T	GRCh38
NC_000021.8:g.34398579C>T , CM000683.1:g.34398579C>T	GRCh37
NC_000021.7:g.33320449C>T	NCBI36
NG_011834.1:g.5341C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-63+245C>T MANE Select	ENSP00000371794.3:n.-63+245C>T
ENST00000333337.3:c.-592C>T	ENSP00000331040.3:n.-592C>T
ENST00000382357.3:c.-63+245C>T	ENSP00000371794.3:n.-63+245C>T
ENST00000430860.1:c.-63+11C>T	ENSP00000391183.1:n.-63+11C>T
NM_005806.3:c.-63+245C>T	NP_005797.1:n.-63+245C>T
XM_005260908.1:c.-63+11C>T	XP_005260965.1:n.-63+11C>T
NM_005806.4:c.-63+245C>T MANE Select	NP_005797.1:n.-63+245C>T