Canonical Allele Identifier: CA2386486257
Gene: OLIG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026219C= , CM000683.2:g.33026219C= GRCh38
NC_000021.8:g.34398527C= , CM000683.1:g.34398527C= GRCh37
NC_000021.7:g.33320397C= NCBI36
NG_011834.1:g.5289C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+193C= MANE Select ENSP00000371794.3:n.-63+193C=
ENST00000333337.3:c.-644C= ENSP00000331040.3:n.-644C=
ENST00000382357.3:c.-63+193C= ENSP00000371794.3:n.-63+193C=
ENST00000430860.1:c.-104C= ENSP00000391183.1:n.-104C=
NM_005806.3:c.-63+193C= NP_005797.1:n.-63+193C=
XM_005260908.1:c.-104C= XP_005260965.1:n.-104C=
NM_005806.4:c.-63+193C= MANE Select NP_005797.1:n.-63+193C=
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