Canonical Allele Identifier: CA2386486333
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1271945901

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026378G>C , CM000683.2:g.33026378G>C GRCh38
NC_000021.8:g.34398686G>C , CM000683.1:g.34398686G>C GRCh37
NC_000021.7:g.33320556G>C NCBI36
NG_011834.1:g.5448G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+352G>C MANE Select ENSP00000371794.3:n.-63+352G>C
ENST00000333337.3:c.-485G>C ENSP00000331040.3:n.-485G>C
ENST00000382357.3:c.-63+352G>C ENSP00000371794.3:n.-63+352G>C
ENST00000430860.1:c.-63+118G>C ENSP00000391183.1:n.-63+118G>C
NM_005806.3:c.-63+352G>C NP_005797.1:n.-63+352G>C
XM_005260908.1:c.-63+118G>C XP_005260965.1:n.-63+118G>C
NM_005806.4:c.-63+352G>C MANE Select NP_005797.1:n.-63+352G>C