Canonical Allele Identifier: CA14859720
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1005573

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026408C>T , CM000683.2:g.33026408C>T GRCh38
NC_000021.8:g.34398716C>T , CM000683.1:g.34398716C>T GRCh37
NC_000021.7:g.33320586C>T NCBI36
NG_011834.1:g.5478C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+382C>T MANE Select ENSP00000371794.3:p.=
ENST00000333337.3:c.-455C>T ENSP00000331040.3:p.=
ENST00000382357.3:c.-63+382C>T ENSP00000371794.3:p.=
ENST00000430860.1:c.-63+148C>T ENSP00000391183.1:p.=
NM_005806.3:c.-63+382C>T NP_005797.1:p.=
XM_005260908.1:c.-63+148C>T XP_005260965.1:p.=
NM_005806.4:c.-63+382C>T MANE Select NP_005797.1:p.=