Canonical Allele Identifier: CA2386486321
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026351T= , CM000683.2:g.33026351T= GRCh38
NC_000021.8:g.34398659T= , CM000683.1:g.34398659T= GRCh37
NC_000021.7:g.33320529T= NCBI36
NG_011834.1:g.5421T=

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+325T= MANE Select ENSP00000371794.3:n.-63+325T=
ENST00000333337.3:c.-512T= ENSP00000331040.3:n.-512T=
ENST00000382357.3:c.-63+325T= ENSP00000371794.3:n.-63+325T=
ENST00000430860.1:c.-63+91T= ENSP00000391183.1:n.-63+91T=
NM_005806.3:c.-63+325T= NP_005797.1:n.-63+325T=
XM_005260908.1:c.-63+91T= XP_005260965.1:n.-63+91T=
NM_005806.4:c.-63+325T= MANE Select NP_005797.1:n.-63+325T=