Canonical Allele Identifier: CA2654283680
Gene: OLIG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026373G>T , CM000683.2:g.33026373G>T GRCh38
NC_000021.8:g.34398681G>T , CM000683.1:g.34398681G>T GRCh37
NC_000021.7:g.33320551G>T NCBI36
NG_011834.1:g.5443G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+347G>T MANE Select ENSP00000371794.3:n.-63+347G>T
ENST00000333337.3:c.-490G>T ENSP00000331040.3:n.-490G>T
ENST00000382357.3:c.-63+347G>T ENSP00000371794.3:n.-63+347G>T
ENST00000430860.1:c.-63+113G>T ENSP00000391183.1:n.-63+113G>T
NM_005806.3:c.-63+347G>T NP_005797.1:n.-63+347G>T
XM_005260908.1:c.-63+113G>T XP_005260965.1:n.-63+113G>T
NM_005806.4:c.-63+347G>T MANE Select NP_005797.1:n.-63+347G>T