Canonical Allele Identifier: CA2654283679
Gene: OLIG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026372_33026373insTA , CM000683.2:g.33026372_33026373insTA GRCh38
NC_000021.8:g.34398680_34398681insTA , CM000683.1:g.34398680_34398681insTA GRCh37
NC_000021.7:g.33320550_33320551insTA NCBI36
NG_011834.1:g.5442_5443insTA

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+346_-63+347insTA MANE Select ENSP00000371794.3:n.-63+346_-63+347insTA
ENST00000333337.3:c.-491_-490insTA ENSP00000331040.3:n.-491_-490insTA
ENST00000382357.3:c.-63+346_-63+347insTA ENSP00000371794.3:n.-63+346_-63+347insTA
ENST00000430860.1:c.-63+112_-63+113insTA ENSP00000391183.1:n.-63+112_-63+113insTA
NM_005806.3:c.-63+346_-63+347insTA NP_005797.1:n.-63+346_-63+347insTA
XM_005260908.1:c.-63+112_-63+113insTA XP_005260965.1:n.-63+112_-63+113insTA
NM_005806.4:c.-63+346_-63+347insTA MANE Select NP_005797.1:n.-63+346_-63+347insTA