Canonical Allele Identifier: CA320091802
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs758061504
MyVariant Identifiers: chr21:g.34398680G>A (hg19) chr21:g.33026372G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026372G>A , CM000683.2:g.33026372G>A GRCh38
NC_000021.8:g.34398680G>A , CM000683.1:g.34398680G>A GRCh37
NC_000021.7:g.33320550G>A NCBI36
NG_011834.1:g.5442G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+346G>A MANE Select ENSP00000371794.3:n.-63+346G>A
ENST00000333337.3:c.-491G>A ENSP00000331040.3:n.-491G>A
ENST00000382357.3:c.-63+346G>A ENSP00000371794.3:n.-63+346G>A
ENST00000430860.1:c.-63+112G>A ENSP00000391183.1:n.-63+112G>A
NM_005806.3:c.-63+346G>A NP_005797.1:n.-63+346G>A
XM_005260908.1:c.-63+112G>A XP_005260965.1:n.-63+112G>A
NM_005806.4:c.-63+346G>A MANE Select NP_005797.1:n.-63+346G>A
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