Canonical Allele Identifier: CA637699518
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1247855875
gnomAD v2: 21-34398754-C-A
gnomAD v3: 21-33026446-C-A
gnomAD v4: 21-33026446-C-A
MyVariant Identifiers: chr21:g.34398754C>A (hg19) chr21:g.33026446C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026446C>A , CM000683.2:g.33026446C>A GRCh38
NC_000021.8:g.34398754C>A , CM000683.1:g.34398754C>A GRCh37
NC_000021.7:g.33320624C>A NCBI36
NG_011834.1:g.5516C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-62-355C>A MANE Select ENSP00000371794.3:n.-62-355C>A
ENST00000333337.3:c.-417C>A ENSP00000331040.3:n.-417C>A
ENST00000382357.3:c.-62-355C>A ENSP00000371794.3:n.-62-355C>A
ENST00000430860.1:c.-63+186C>A ENSP00000391183.1:n.-63+186C>A
NM_005806.3:c.-62-355C>A NP_005797.1:n.-62-355C>A
XM_005260908.1:c.-63+186C>A XP_005260965.1:n.-63+186C>A
NM_005806.4:c.-62-355C>A MANE Select NP_005797.1:n.-62-355C>A
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