Canonical Allele Identifier: CA2386486402
Gene: OLIG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026514T= , CM000683.2:g.33026514T= GRCh38
NC_000021.8:g.34398822T= , CM000683.1:g.34398822T= GRCh37
NC_000021.7:g.33320692T= NCBI36
NG_011834.1:g.5584T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-62-287T= MANE Select ENSP00000371794.3:n.-62-287T=
ENST00000333337.3:c.-349T= ENSP00000331040.3:n.-349T=
ENST00000382357.3:c.-62-287T= ENSP00000371794.3:n.-62-287T=
ENST00000430860.1:c.-63+254T= ENSP00000391183.1:n.-63+254T=
NM_005806.3:c.-62-287T= NP_005797.1:n.-62-287T=
XM_005260908.1:c.-63+254T= XP_005260965.1:n.-63+254T=
NM_005806.4:c.-62-287T= MANE Select NP_005797.1:n.-62-287T=
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