Canonical Allele Identifier: CA2386486413
Gene: OLIG2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026525C= , CM000683.2:g.33026525C= GRCh38
NC_000021.8:g.34398833C= , CM000683.1:g.34398833C= GRCh37
NC_000021.7:g.33320703C= NCBI36
NG_011834.1:g.5595C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-62-276C= MANE Select ENSP00000371794.3:n.-62-276C=
ENST00000333337.3:c.-338C= ENSP00000331040.3:n.-338C=
ENST00000382357.3:c.-62-276C= ENSP00000371794.3:n.-62-276C=
ENST00000430860.1:c.-63+265C= ENSP00000391183.1:n.-63+265C=
NM_005806.3:c.-62-276C= NP_005797.1:n.-62-276C=
XM_005260908.1:c.-63+265C= XP_005260965.1:n.-63+265C=
NM_005806.4:c.-62-276C= MANE Select NP_005797.1:n.-62-276C=
Search 100 bp 5'
Search 100 bp 3'