Canonical Allele Identifier: CA1021917137
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981068904
gnomAD v3: 21-33026295-G-T
gnomAD v4: 21-33026295-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026295G>T , CM000683.2:g.33026295G>T GRCh38
NC_000021.8:g.34398603G>T , CM000683.1:g.34398603G>T GRCh37
NC_000021.7:g.33320473G>T NCBI36
NG_011834.1:g.5365G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+269G>T MANE Select ENSP00000371794.3:n.-63+269G>T
ENST00000333337.3:c.-568G>T ENSP00000331040.3:n.-568G>T
ENST00000382357.3:c.-63+269G>T ENSP00000371794.3:n.-63+269G>T
ENST00000430860.1:c.-63+35G>T ENSP00000391183.1:n.-63+35G>T
NM_005806.3:c.-63+269G>T NP_005797.1:n.-63+269G>T
XM_005260908.1:c.-63+35G>T XP_005260965.1:n.-63+35G>T
NM_005806.4:c.-63+269G>T MANE Select NP_005797.1:n.-63+269G>T
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