Canonical Allele Identifier: CA14859720
Gene: OLIG2 HGNC NCBI
MyVariant.info:
GRCh38 chr21:g.33026408C>T
GRCh37 chr21:g.34398716C>T
gnomAD v2:
21:34398716 C / T
gnomAD v3:
21:33026408 C / T
gnomAD v4:
chr21-33026408-C-T
Joint Max Group AF 0.84780876 (AFR)
Genomes Max Group AF 0.84814887 (AFR)
Exomes Max Group AF 0.69524035 (AFR)
dbSNP:
1005573
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026408C>T , CM000683.2:g.33026408C>T GRCh38
NC_000021.8:g.34398716C>T , CM000683.1:g.34398716C>T GRCh37
NC_000021.7:g.33320586C>T NCBI36
NG_011834.1:g.5478C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+382C>T MANE Select ENSP00000371794.3:n.-63+382C>T
ENST00000333337.3:c.-455C>T ENSP00000331040.3:n.-455C>T
ENST00000382357.3:c.-63+382C>T ENSP00000371794.3:n.-63+382C>T
ENST00000430860.1:c.-63+148C>T ENSP00000391183.1:n.-63+148C>T
NM_005806.3:c.-63+382C>T NP_005797.1:n.-63+382C>T
XM_005260908.1:c.-63+148C>T XP_005260965.1:n.-63+148C>T
NM_005806.4:c.-63+382C>T MANE Select NP_005797.1:n.-63+382C>T
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