Canonical Allele Identifier: CA2386486287
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981068310
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026282G>C , CM000683.2:g.33026282G>C GRCh38
NC_000021.8:g.34398590G>C , CM000683.1:g.34398590G>C GRCh37
NC_000021.7:g.33320460G>C NCBI36
NG_011834.1:g.5352G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+256G>C MANE Select ENSP00000371794.3:n.-63+256G>C
ENST00000333337.3:c.-581G>C ENSP00000331040.3:n.-581G>C
ENST00000382357.3:c.-63+256G>C ENSP00000371794.3:n.-63+256G>C
ENST00000430860.1:c.-63+22G>C ENSP00000391183.1:n.-63+22G>C
NM_005806.3:c.-63+256G>C NP_005797.1:n.-63+256G>C
XM_005260908.1:c.-63+22G>C XP_005260965.1:n.-63+22G>C
NM_005806.4:c.-63+256G>C MANE Select NP_005797.1:n.-63+256G>C
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