Canonical Allele Identifier: CA2817737845
Gene: OLIG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026392del , CM000683.2:g.33026392del GRCh38
NC_000021.8:g.34398700del , CM000683.1:g.34398700del GRCh37
NC_000021.7:g.33320570del NCBI36
NG_011834.1:g.5462del

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+366del MANE Select ENSP00000371794.3:n.-63+366del
ENST00000333337.3:c.-471del ENSP00000331040.3:n.-471del
ENST00000382357.3:c.-63+366del ENSP00000371794.3:n.-63+366del
ENST00000430860.1:c.-63+132del ENSP00000391183.1:n.-63+132del
NM_005806.3:c.-63+366del NP_005797.1:n.-63+366del
XM_005260908.1:c.-63+132del XP_005260965.1:n.-63+132del
NM_005806.4:c.-63+366del MANE Select NP_005797.1:n.-63+366del