Canonical Allele Identifier: CA2654283737
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026400-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026400T>G , CM000683.2:g.33026400T>G GRCh38
NC_000021.8:g.34398708T>G , CM000683.1:g.34398708T>G GRCh37
NC_000021.7:g.33320578T>G NCBI36
NG_011834.1:g.5470T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+374T>G MANE Select ENSP00000371794.3:n.-63+374T>G
ENST00000333337.3:c.-463T>G ENSP00000331040.3:n.-463T>G
ENST00000382357.3:c.-63+374T>G ENSP00000371794.3:n.-63+374T>G
ENST00000430860.1:c.-63+140T>G ENSP00000391183.1:n.-63+140T>G
NM_005806.3:c.-63+374T>G NP_005797.1:n.-63+374T>G
XM_005260908.1:c.-63+140T>G XP_005260965.1:n.-63+140T>G
NM_005806.4:c.-63+374T>G MANE Select NP_005797.1:n.-63+374T>G
Search 100 bp 5'
Search 100 bp 3'