Canonical Allele Identifier: CA2386486347
Gene: OLIG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026399G= , CM000683.2:g.33026399G= GRCh38
NC_000021.8:g.34398707G= , CM000683.1:g.34398707G= GRCh37
NC_000021.7:g.33320577G= NCBI36
NG_011834.1:g.5469G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+373G= MANE Select ENSP00000371794.3:n.-63+373G=
ENST00000333337.3:c.-464G= ENSP00000331040.3:n.-464G=
ENST00000382357.3:c.-63+373G= ENSP00000371794.3:n.-63+373G=
ENST00000430860.1:c.-63+139G= ENSP00000391183.1:n.-63+139G=
NM_005806.3:c.-63+373G= NP_005797.1:n.-63+373G=
XM_005260908.1:c.-63+139G= XP_005260965.1:n.-63+139G=
NM_005806.4:c.-63+373G= MANE Select NP_005797.1:n.-63+373G=
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