Allele Registry

Canonical Allele Identifier: CA10005266

Gene: OLIG2 HGNC NCBI

Linked Data - Expert Curation

COSMIC:

COSM3766647 (not active)

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr21:g.33027093A>G

GRCh37 chr21:g.34399401A>G

Linked Data - Sequence & Population

gnomAD v2:

21:34399401 A / G

gnomAD v3:

21:33027093 A / G

gnomAD v4:

chr21-33027093-A-G

Joint Max Group AF 0.57474558 (NFE)

Genomes Max Group AF 0.56692932 (NFE)

Exomes Max Group AF 0.57496835 (NFE)

Linked Data - NCBI & NCI

dbSNP:

762178

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33027093A>G , CM000683.2:g.33027093A>G	GRCh38
NC_000021.8:g.34399401A>G , CM000683.1:g.34399401A>G	GRCh37
NC_000021.7:g.33321271A>G	NCBI36
NG_011834.1:g.6163A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.231A>G MANE Select	ENSP00000371794.3:p.Ser77=
ENST00000333337.3:c.231A>G	ENSP00000331040.3:p.Ser77=
ENST00000382357.3:c.231A>G	ENSP00000371794.3:p.Ser77=
NM_005806.3:c.231A>G	NP_005797.1:p.Ser77=
XM_005260908.1:c.231A>G	XP_005260965.1:p.Ser77=
NM_005806.4:c.231A>G MANE Select	NP_005797.1:p.Ser77=

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