Canonical Allele Identifier: CA2654283532
Gene: OLIG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026211C>A , CM000683.2:g.33026211C>A GRCh38
NC_000021.8:g.34398519C>A , CM000683.1:g.34398519C>A GRCh37
NC_000021.7:g.33320389C>A NCBI36
NG_011834.1:g.5281C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+185C>A MANE Select ENSP00000371794.3:n.-63+185C>A
ENST00000333337.3:c.-652C>A ENSP00000331040.3:n.-652C>A
ENST00000382357.3:c.-63+185C>A ENSP00000371794.3:n.-63+185C>A
ENST00000430860.1:c.-112C>A ENSP00000391183.1:n.-112C>A
NM_005806.3:c.-63+185C>A NP_005797.1:n.-63+185C>A
XM_005260908.1:c.-112C>A XP_005260965.1:n.-112C>A
NM_005806.4:c.-63+185C>A MANE Select NP_005797.1:n.-63+185C>A