Canonical Allele Identifier: CA2386486460
Gene: OLIG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026608G= , CM000683.2:g.33026608G= GRCh38
NC_000021.8:g.34398916G= , CM000683.1:g.34398916G= GRCh37
NC_000021.7:g.33320786G= NCBI36
NG_011834.1:g.5678G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-62-193G= MANE Select ENSP00000371794.3:n.-62-193G=
ENST00000333337.3:c.-255G= ENSP00000331040.3:n.-255G=
ENST00000382357.3:c.-62-193G= ENSP00000371794.3:n.-62-193G=
ENST00000430860.1:c.-62-193G= ENSP00000391183.1:n.-62-193G=
NM_005806.3:c.-62-193G= NP_005797.1:n.-62-193G=
XM_005260908.1:c.-62-193G= XP_005260965.1:n.-62-193G=
NM_005806.4:c.-62-193G= MANE Select NP_005797.1:n.-62-193G=
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