Canonical Allele Identifier: CA637699516
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1326328917

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026429dup , CM000683.2:g.33026429dup GRCh38
NC_000021.8:g.34398737dup , CM000683.1:g.34398737dup GRCh37
NC_000021.7:g.33320607dup NCBI36
NG_011834.1:g.5499dup

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-62-372dup MANE Select ENSP00000371794.3:n.-62-372dup
ENST00000333337.3:c.-434dup ENSP00000331040.3:n.-434dup
ENST00000382357.3:c.-62-372dup ENSP00000371794.3:n.-62-372dup
ENST00000430860.1:c.-63+169dup ENSP00000391183.1:n.-63+169dup
NM_005806.3:c.-62-372dup NP_005797.1:n.-62-372dup
XM_005260908.1:c.-63+169dup XP_005260965.1:n.-63+169dup
NM_005806.4:c.-62-372dup MANE Select NP_005797.1:n.-62-372dup