Canonical Allele Identifier: CA2386486369
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026442C= , CM000683.2:g.33026442C= GRCh38
NC_000021.8:g.34398750C= , CM000683.1:g.34398750C= GRCh37
NC_000021.7:g.33320620C= NCBI36
NG_011834.1:g.5512C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-62-359C= MANE Select ENSP00000371794.3:n.-62-359C=
ENST00000333337.3:c.-421C= ENSP00000331040.3:n.-421C=
ENST00000382357.3:c.-62-359C= ENSP00000371794.3:n.-62-359C=
ENST00000430860.1:c.-63+182C= ENSP00000391183.1:n.-63+182C=
NM_005806.3:c.-62-359C= NP_005797.1:n.-62-359C=
XM_005260908.1:c.-63+182C= XP_005260965.1:n.-63+182C=
NM_005806.4:c.-62-359C= MANE Select NP_005797.1:n.-62-359C=