Canonical Allele Identifier: CA2386486366
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981073909

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026433A>G , CM000683.2:g.33026433A>G GRCh38
NC_000021.8:g.34398741A>G , CM000683.1:g.34398741A>G GRCh37
NC_000021.7:g.33320611A>G NCBI36
NG_011834.1:g.5503A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-62-368A>G MANE Select ENSP00000371794.3:n.-62-368A>G
ENST00000333337.3:c.-430A>G ENSP00000331040.3:n.-430A>G
ENST00000382357.3:c.-62-368A>G ENSP00000371794.3:n.-62-368A>G
ENST00000430860.1:c.-63+173A>G ENSP00000391183.1:n.-63+173A>G
NM_005806.3:c.-62-368A>G NP_005797.1:n.-62-368A>G
XM_005260908.1:c.-63+173A>G XP_005260965.1:n.-63+173A>G
NM_005806.4:c.-62-368A>G MANE Select NP_005797.1:n.-62-368A>G