Canonical Allele Identifier: CA637699519

Gene: OLIG2

Linked Data

• dbSNP Id: rs1465021231
• gnomAD v2: 21-34398774-G-C
• gnomAD v3: 21-33026466-G-C
• gnomAD v4: 21-33026466-G-C
• MyVariant Identifiers: chr21:g.34398774G>C (hg19) ; chr21:g.33026466G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026466G>C , CM000683.2:g.33026466G>C	GRCh38
NC_000021.8:g.34398774G>C , CM000683.1:g.34398774G>C	GRCh37
NC_000021.7:g.33320644G>C	NCBI36
NG_011834.1:g.5536G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-62-335G>C MANE Select	ENSP00000371794.3:n.-62-335G>C
ENST00000333337.3:c.-397G>C	ENSP00000331040.3:n.-397G>C
ENST00000382357.3:c.-62-335G>C	ENSP00000371794.3:n.-62-335G>C
ENST00000430860.1:c.-63+206G>C	ENSP00000391183.1:n.-63+206G>C
NM_005806.3:c.-62-335G>C	NP_005797.1:n.-62-335G>C
XM_005260908.1:c.-63+206G>C	XP_005260965.1:n.-63+206G>C
NM_005806.4:c.-62-335G>C MANE Select	NP_005797.1:n.-62-335G>C