Canonical Allele Identifier: CA2386486298
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981068995
gnomAD v4: 21-33026302-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026302G>A , CM000683.2:g.33026302G>A GRCh38
NC_000021.8:g.34398610G>A , CM000683.1:g.34398610G>A GRCh37
NC_000021.7:g.33320480G>A NCBI36
NG_011834.1:g.5372G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+276G>A MANE Select ENSP00000371794.3:n.-63+276G>A
ENST00000333337.3:c.-561G>A ENSP00000331040.3:n.-561G>A
ENST00000382357.3:c.-63+276G>A ENSP00000371794.3:n.-63+276G>A
ENST00000430860.1:c.-63+42G>A ENSP00000391183.1:n.-63+42G>A
NM_005806.3:c.-63+276G>A NP_005797.1:n.-63+276G>A
XM_005260908.1:c.-63+42G>A XP_005260965.1:n.-63+42G>A
NM_005806.4:c.-63+276G>A MANE Select NP_005797.1:n.-63+276G>A
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