Canonical Allele Identifier: CA2386486256
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1209644321

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026219C>G , CM000683.2:g.33026219C>G GRCh38
NC_000021.8:g.34398527C>G , CM000683.1:g.34398527C>G GRCh37
NC_000021.7:g.33320397C>G NCBI36
NG_011834.1:g.5289C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+193C>G MANE Select ENSP00000371794.3:n.-63+193C>G
ENST00000333337.3:c.-644C>G ENSP00000331040.3:n.-644C>G
ENST00000382357.3:c.-63+193C>G ENSP00000371794.3:n.-63+193C>G
ENST00000430860.1:c.-104C>G ENSP00000391183.1:n.-104C>G
NM_005806.3:c.-63+193C>G NP_005797.1:n.-63+193C>G
XM_005260908.1:c.-104C>G XP_005260965.1:n.-104C>G
NM_005806.4:c.-63+193C>G MANE Select NP_005797.1:n.-63+193C>G