Canonical Allele Identifier: CA637699510

Gene: OLIG2

Linked Data

• dbSNP Id: rs1169127224
• gnomAD v2: 21-34398562-T-C
• gnomAD v3: 21-33026254-T-C
• gnomAD v4: 21-33026254-T-C
• MyVariant Identifiers: chr21:g.34398562T>C (hg19) ; chr21:g.33026254T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026254T>C , CM000683.2:g.33026254T>C	GRCh38
NC_000021.8:g.34398562T>C , CM000683.1:g.34398562T>C	GRCh37
NC_000021.7:g.33320432T>C	NCBI36
NG_011834.1:g.5324T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+228T>C MANE Select	ENSP00000371794.3:n.-63+228T>C
ENST00000333337.3:c.-609T>C	ENSP00000331040.3:n.-609T>C
ENST00000382357.3:c.-63+228T>C	ENSP00000371794.3:n.-63+228T>C
ENST00000430860.1:c.-69T>C	ENSP00000391183.1:n.-69T>C
NM_005806.3:c.-63+228T>C	NP_005797.1:n.-63+228T>C
XM_005260908.1:c.-69T>C	XP_005260965.1:n.-69T>C
NM_005806.4:c.-63+228T>C MANE Select	NP_005797.1:n.-63+228T>C