Canonical Allele Identifier: CA2654283622
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026317-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026317C>G , CM000683.2:g.33026317C>G GRCh38
NC_000021.8:g.34398625C>G , CM000683.1:g.34398625C>G GRCh37
NC_000021.7:g.33320495C>G NCBI36
NG_011834.1:g.5387C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+291C>G MANE Select ENSP00000371794.3:n.-63+291C>G
ENST00000333337.3:c.-546C>G ENSP00000331040.3:n.-546C>G
ENST00000382357.3:c.-63+291C>G ENSP00000371794.3:n.-63+291C>G
ENST00000430860.1:c.-63+57C>G ENSP00000391183.1:n.-63+57C>G
NM_005806.3:c.-63+291C>G NP_005797.1:n.-63+291C>G
XM_005260908.1:c.-63+57C>G XP_005260965.1:n.-63+57C>G
NM_005806.4:c.-63+291C>G MANE Select NP_005797.1:n.-63+291C>G
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