Canonical Allele Identifier: CA320091790
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs972037300
gnomAD v2: 21-34398557-C-G
gnomAD v3: 21-33026249-C-G
gnomAD v4: 21-33026249-C-G
MyVariant Identifiers: chr21:g.34398557C>G (hg19) chr21:g.33026249C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026249C>G , CM000683.2:g.33026249C>G GRCh38
NC_000021.8:g.34398557C>G , CM000683.1:g.34398557C>G GRCh37
NC_000021.7:g.33320427C>G NCBI36
NG_011834.1:g.5319C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+223C>G MANE Select ENSP00000371794.3:n.-63+223C>G
ENST00000333337.3:c.-614C>G ENSP00000331040.3:n.-614C>G
ENST00000382357.3:c.-63+223C>G ENSP00000371794.3:n.-63+223C>G
ENST00000430860.1:c.-74C>G ENSP00000391183.1:n.-74C>G
NM_005806.3:c.-63+223C>G NP_005797.1:n.-63+223C>G
XM_005260908.1:c.-74C>G XP_005260965.1:n.-74C>G
NM_005806.4:c.-63+223C>G MANE Select NP_005797.1:n.-63+223C>G
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