Canonical Allele Identifier: CA2386486255
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981065783
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026215A>C , CM000683.2:g.33026215A>C GRCh38
NC_000021.8:g.34398523A>C , CM000683.1:g.34398523A>C GRCh37
NC_000021.7:g.33320393A>C NCBI36
NG_011834.1:g.5285A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+189A>C MANE Select ENSP00000371794.3:n.-63+189A>C
ENST00000333337.3:c.-648A>C ENSP00000331040.3:n.-648A>C
ENST00000382357.3:c.-63+189A>C ENSP00000371794.3:n.-63+189A>C
ENST00000430860.1:c.-108A>C ENSP00000391183.1:n.-108A>C
NM_005806.3:c.-63+189A>C NP_005797.1:n.-63+189A>C
XM_005260908.1:c.-108A>C XP_005260965.1:n.-108A>C
NM_005806.4:c.-63+189A>C MANE Select NP_005797.1:n.-63+189A>C
Search 100 bp 5'
Search 100 bp 3'