Canonical Allele Identifier: CA2386486275
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981067524
gnomAD v4: 21-33026262-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026262T>A , CM000683.2:g.33026262T>A GRCh38
NC_000021.8:g.34398570T>A , CM000683.1:g.34398570T>A GRCh37
NC_000021.7:g.33320440T>A NCBI36
NG_011834.1:g.5332T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+236T>A MANE Select ENSP00000371794.3:n.-63+236T>A
ENST00000333337.3:c.-601T>A ENSP00000331040.3:n.-601T>A
ENST00000382357.3:c.-63+236T>A ENSP00000371794.3:n.-63+236T>A
ENST00000430860.1:c.-63+2T>A ENSP00000391183.1:n.-63+2T>A
NM_005806.3:c.-63+236T>A NP_005797.1:n.-63+236T>A
XM_005260908.1:c.-63+2T>A XP_005260965.1:n.-63+2T>A
NM_005806.4:c.-63+236T>A MANE Select NP_005797.1:n.-63+236T>A
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