Canonical Allele Identifier: CA2737571593
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1475248898
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+305G>C MANE Select ENSP00000371794.3:n.-63+305G>C
ENST00000333337.3:c.-532G>C ENSP00000331040.3:n.-532G>C
ENST00000382357.3:c.-63+305G>C ENSP00000371794.3:n.-63+305G>C
ENST00000430860.1:c.-63+71G>C ENSP00000391183.1:n.-63+71G>C
NM_005806.3:c.-63+305G>C NP_005797.1:n.-63+305G>C
XM_005260908.1:c.-63+71G>C XP_005260965.1:n.-63+71G>C
NM_005806.4:c.-63+305G>C MANE Select NP_005797.1:n.-63+305G>C
Search 100 bp 5'
Search 100 bp 3'