Canonical Allele Identifier: CA2654283611
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026307-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026307C>T , CM000683.2:g.33026307C>T GRCh38
NC_000021.8:g.34398615C>T , CM000683.1:g.34398615C>T GRCh37
NC_000021.7:g.33320485C>T NCBI36
NG_011834.1:g.5377C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+281C>T MANE Select ENSP00000371794.3:n.-63+281C>T
ENST00000333337.3:c.-556C>T ENSP00000331040.3:n.-556C>T
ENST00000382357.3:c.-63+281C>T ENSP00000371794.3:n.-63+281C>T
ENST00000430860.1:c.-63+47C>T ENSP00000391183.1:n.-63+47C>T
NM_005806.3:c.-63+281C>T NP_005797.1:n.-63+281C>T
XM_005260908.1:c.-63+47C>T XP_005260965.1:n.-63+47C>T
NM_005806.4:c.-63+281C>T MANE Select NP_005797.1:n.-63+281C>T
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