Canonical Allele Identifier: CA2654283595
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026292-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026292A>G , CM000683.2:g.33026292A>G GRCh38
NC_000021.8:g.34398600A>G , CM000683.1:g.34398600A>G GRCh37
NC_000021.7:g.33320470A>G NCBI36
NG_011834.1:g.5362A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+266A>G MANE Select ENSP00000371794.3:n.-63+266A>G
ENST00000333337.3:c.-571A>G ENSP00000331040.3:n.-571A>G
ENST00000382357.3:c.-63+266A>G ENSP00000371794.3:n.-63+266A>G
ENST00000430860.1:c.-63+32A>G ENSP00000391183.1:n.-63+32A>G
NM_005806.3:c.-63+266A>G NP_005797.1:n.-63+266A>G
XM_005260908.1:c.-63+32A>G XP_005260965.1:n.-63+32A>G
NM_005806.4:c.-63+266A>G MANE Select NP_005797.1:n.-63+266A>G
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