Canonical Allele Identifier: CA2386486392
Gene: OLIG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026492T= , CM000683.2:g.33026492T= GRCh38
NC_000021.8:g.34398800T= , CM000683.1:g.34398800T= GRCh37
NC_000021.7:g.33320670T= NCBI36
NG_011834.1:g.5562T=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-62-309T= MANE Select ENSP00000371794.3:n.-62-309T=
ENST00000333337.3:c.-371T= ENSP00000331040.3:n.-371T=
ENST00000382357.3:c.-62-309T= ENSP00000371794.3:n.-62-309T=
ENST00000430860.1:c.-63+232T= ENSP00000391183.1:n.-63+232T=
NM_005806.3:c.-62-309T= NP_005797.1:n.-62-309T=
XM_005260908.1:c.-63+232T= XP_005260965.1:n.-63+232T=
NM_005806.4:c.-62-309T= MANE Select NP_005797.1:n.-62-309T=
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