Canonical Allele Identifier: CA748767296
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1475248898

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026331G>A , CM000683.2:g.33026331G>A GRCh38
NC_000021.8:g.34398639G>A , CM000683.1:g.34398639G>A GRCh37
NC_000021.7:g.33320509G>A NCBI36
NG_011834.1:g.5401G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+305G>A MANE Select ENSP00000371794.3:n.-63+305G>A
ENST00000333337.3:c.-532G>A ENSP00000331040.3:n.-532G>A
ENST00000382357.3:c.-63+305G>A ENSP00000371794.3:n.-63+305G>A
ENST00000430860.1:c.-63+71G>A ENSP00000391183.1:n.-63+71G>A
NM_005806.3:c.-63+305G>A NP_005797.1:n.-63+305G>A
XM_005260908.1:c.-63+71G>A XP_005260965.1:n.-63+71G>A
NM_005806.4:c.-63+305G>A MANE Select NP_005797.1:n.-63+305G>A