Canonical Allele Identifier: CA2654283579
Gene: OLIG2 HGNC NCBI

Linked Data

gnomAD v4: 21-33026277-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026277C>A , CM000683.2:g.33026277C>A GRCh38
NC_000021.8:g.34398585C>A , CM000683.1:g.34398585C>A GRCh37
NC_000021.7:g.33320455C>A NCBI36
NG_011834.1:g.5347C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382357.4:c.-63+251C>A MANE Select ENSP00000371794.3:n.-63+251C>A
ENST00000333337.3:c.-586C>A ENSP00000331040.3:n.-586C>A
ENST00000382357.3:c.-63+251C>A ENSP00000371794.3:n.-63+251C>A
ENST00000430860.1:c.-63+17C>A ENSP00000391183.1:n.-63+17C>A
NM_005806.3:c.-63+251C>A NP_005797.1:n.-63+251C>A
XM_005260908.1:c.-63+17C>A XP_005260965.1:n.-63+17C>A
NM_005806.4:c.-63+251C>A MANE Select NP_005797.1:n.-63+251C>A
Search 100 bp 5'
Search 100 bp 3'