Canonical Allele Identifier: CA2386486241
Gene: OLIG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026180A= , CM000683.2:g.33026180A= GRCh38
NC_000021.8:g.34398488A= , CM000683.1:g.34398488A= GRCh37
NC_000021.7:g.33320358A= NCBI36
NG_011834.1:g.5250A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+154A= MANE Select ENSP00000371794.3:n.-63+154A=
ENST00000333337.3:c.-683A= ENSP00000331040.3:n.-683A=
ENST00000382357.3:c.-63+154A= ENSP00000371794.3:n.-63+154A=
ENST00000430860.1:c.-143A= ENSP00000391183.1:n.-143A=
NM_005806.3:c.-63+154A= NP_005797.1:n.-63+154A=
XM_005260908.1:c.-143A= XP_005260965.1:n.-143A=
NM_005806.4:c.-63+154A= MANE Select NP_005797.1:n.-63+154A=
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