Canonical Allele Identifier: CA2654283676
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026371-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026371T>C , CM000683.2:g.33026371T>C GRCh38
NC_000021.8:g.34398679T>C , CM000683.1:g.34398679T>C GRCh37
NC_000021.7:g.33320549T>C NCBI36
NG_011834.1:g.5441T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+345T>C MANE Select ENSP00000371794.3:n.-63+345T>C
ENST00000333337.3:c.-492T>C ENSP00000331040.3:n.-492T>C
ENST00000382357.3:c.-63+345T>C ENSP00000371794.3:n.-63+345T>C
ENST00000430860.1:c.-63+111T>C ENSP00000391183.1:n.-63+111T>C
NM_005806.3:c.-63+345T>C NP_005797.1:n.-63+345T>C
XM_005260908.1:c.-63+111T>C XP_005260965.1:n.-63+111T>C
NM_005806.4:c.-63+345T>C MANE Select NP_005797.1:n.-63+345T>C
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