Canonical Allele Identifier: CA2386486397
Gene: OLIG2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026503A= , CM000683.2:g.33026503A= GRCh38
NC_000021.8:g.34398811A= , CM000683.1:g.34398811A= GRCh37
NC_000021.7:g.33320681A= NCBI36
NG_011834.1:g.5573A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-62-298A= MANE Select ENSP00000371794.3:n.-62-298A=
ENST00000333337.3:c.-360A= ENSP00000331040.3:n.-360A=
ENST00000382357.3:c.-62-298A= ENSP00000371794.3:n.-62-298A=
ENST00000430860.1:c.-63+243A= ENSP00000391183.1:n.-63+243A=
NM_005806.3:c.-62-298A= NP_005797.1:n.-62-298A=
XM_005260908.1:c.-63+243A= XP_005260965.1:n.-63+243A=
NM_005806.4:c.-62-298A= MANE Select NP_005797.1:n.-62-298A=
Search 100 bp 5'
Search 100 bp 3'