Canonical Allele Identifier: CA637699511
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1413768860
gnomAD v2: 21-34398599-C-T
gnomAD v3: 21-33026291-C-T
gnomAD v4: 21-33026291-C-T
MyVariant Identifiers: chr21:g.34398599C>T (hg19) chr21:g.33026291C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026291C>T , CM000683.2:g.33026291C>T GRCh38
NC_000021.8:g.34398599C>T , CM000683.1:g.34398599C>T GRCh37
NC_000021.7:g.33320469C>T NCBI36
NG_011834.1:g.5361C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+265C>T MANE Select ENSP00000371794.3:n.-63+265C>T
ENST00000333337.3:c.-572C>T ENSP00000331040.3:n.-572C>T
ENST00000382357.3:c.-63+265C>T ENSP00000371794.3:n.-63+265C>T
ENST00000430860.1:c.-63+31C>T ENSP00000391183.1:n.-63+31C>T
NM_005806.3:c.-63+265C>T NP_005797.1:n.-63+265C>T
XM_005260908.1:c.-63+31C>T XP_005260965.1:n.-63+31C>T
NM_005806.4:c.-63+265C>T MANE Select NP_005797.1:n.-63+265C>T
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