Canonical Allele Identifier: CA748767344
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1345958282

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026412A>G , CM000683.2:g.33026412A>G GRCh38
NC_000021.8:g.34398720A>G , CM000683.1:g.34398720A>G GRCh37
NC_000021.7:g.33320590A>G NCBI36
NG_011834.1:g.5482A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+386A>G MANE Select ENSP00000371794.3:n.-63+386A>G
ENST00000333337.3:c.-451A>G ENSP00000331040.3:n.-451A>G
ENST00000382357.3:c.-63+386A>G ENSP00000371794.3:n.-63+386A>G
ENST00000430860.1:c.-63+152A>G ENSP00000391183.1:n.-63+152A>G
NM_005806.3:c.-63+386A>G NP_005797.1:n.-63+386A>G
XM_005260908.1:c.-63+152A>G XP_005260965.1:n.-63+152A>G
NM_005806.4:c.-63+386A>G MANE Select NP_005797.1:n.-63+386A>G