Canonical Allele Identifier: CA320091796
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs956392574

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026313G>A , CM000683.2:g.33026313G>A GRCh38
NC_000021.8:g.34398621G>A , CM000683.1:g.34398621G>A GRCh37
NC_000021.7:g.33320491G>A NCBI36
NG_011834.1:g.5383G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+287G>A MANE Select ENSP00000371794.3:n.-63+287G>A
ENST00000333337.3:c.-550G>A ENSP00000331040.3:n.-550G>A
ENST00000382357.3:c.-63+287G>A ENSP00000371794.3:n.-63+287G>A
ENST00000430860.1:c.-63+53G>A ENSP00000391183.1:n.-63+53G>A
NM_005806.3:c.-63+287G>A NP_005797.1:n.-63+287G>A
XM_005260908.1:c.-63+53G>A XP_005260965.1:n.-63+53G>A
NM_005806.4:c.-63+287G>A MANE Select NP_005797.1:n.-63+287G>A