Canonical Allele Identifier: CA2817737839

Gene: OLIG2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026337G>C , CM000683.2:g.33026337G>C	GRCh38
NC_000021.8:g.34398645G>C , CM000683.1:g.34398645G>C	GRCh37
NC_000021.7:g.33320515G>C	NCBI36
NG_011834.1:g.5407G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-63+311G>C MANE Select	ENSP00000371794.3:n.-63+311G>C
ENST00000333337.3:c.-526G>C	ENSP00000331040.3:n.-526G>C
ENST00000382357.3:c.-63+311G>C	ENSP00000371794.3:n.-63+311G>C
ENST00000430860.1:c.-63+77G>C	ENSP00000391183.1:n.-63+77G>C
NM_005806.3:c.-63+311G>C	NP_005797.1:n.-63+311G>C
XM_005260908.1:c.-63+77G>C	XP_005260965.1:n.-63+77G>C
NM_005806.4:c.-63+311G>C MANE Select	NP_005797.1:n.-63+311G>C