Canonical Allele Identifier: CA748767223
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1156719276
MyVariant Identifiers: chr21:g.34398488A>G (hg19) chr21:g.33026180A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026180A>G , CM000683.2:g.33026180A>G GRCh38
NC_000021.8:g.34398488A>G , CM000683.1:g.34398488A>G GRCh37
NC_000021.7:g.33320358A>G NCBI36
NG_011834.1:g.5250A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+154A>G MANE Select ENSP00000371794.3:n.-63+154A>G
ENST00000333337.3:c.-683A>G ENSP00000331040.3:n.-683A>G
ENST00000382357.3:c.-63+154A>G ENSP00000371794.3:n.-63+154A>G
ENST00000430860.1:c.-143A>G ENSP00000391183.1:n.-143A>G
NM_005806.3:c.-63+154A>G NP_005797.1:n.-63+154A>G
XM_005260908.1:c.-143A>G XP_005260965.1:n.-143A>G
NM_005806.4:c.-63+154A>G MANE Select NP_005797.1:n.-63+154A>G
Search 100 bp 5'
Search 100 bp 3'