Canonical Allele Identifier: CA2654283865
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026498-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026498C>T , CM000683.2:g.33026498C>T GRCh38
NC_000021.8:g.34398806C>T , CM000683.1:g.34398806C>T GRCh37
NC_000021.7:g.33320676C>T NCBI36
NG_011834.1:g.5568C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-62-303C>T MANE Select ENSP00000371794.3:n.-62-303C>T
ENST00000333337.3:c.-365C>T ENSP00000331040.3:n.-365C>T
ENST00000382357.3:c.-62-303C>T ENSP00000371794.3:n.-62-303C>T
ENST00000430860.1:c.-63+238C>T ENSP00000391183.1:n.-63+238C>T
NM_005806.3:c.-62-303C>T NP_005797.1:n.-62-303C>T
XM_005260908.1:c.-63+238C>T XP_005260965.1:n.-63+238C>T
NM_005806.4:c.-62-303C>T MANE Select NP_005797.1:n.-62-303C>T
Search 100 bp 5'
Search 100 bp 3'