Canonical Allele Identifier: CA2654283713
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026390-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026390A>C , CM000683.2:g.33026390A>C GRCh38
NC_000021.8:g.34398698A>C , CM000683.1:g.34398698A>C GRCh37
NC_000021.7:g.33320568A>C NCBI36
NG_011834.1:g.5460A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+364A>C MANE Select ENSP00000371794.3:n.-63+364A>C
ENST00000333337.3:c.-473A>C ENSP00000331040.3:n.-473A>C
ENST00000382357.3:c.-63+364A>C ENSP00000371794.3:n.-63+364A>C
ENST00000430860.1:c.-63+130A>C ENSP00000391183.1:n.-63+130A>C
NM_005806.3:c.-63+364A>C NP_005797.1:n.-63+364A>C
XM_005260908.1:c.-63+130A>C XP_005260965.1:n.-63+130A>C
NM_005806.4:c.-63+364A>C MANE Select NP_005797.1:n.-63+364A>C
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