Canonical Allele Identifier: CA2654283506

Gene: OLIG2

Linked Data

• gnomAD v4: 21-33026179-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026179C>T , CM000683.2:g.33026179C>T	GRCh38
NC_000021.8:g.34398487C>T , CM000683.1:g.34398487C>T	GRCh37
NC_000021.7:g.33320357C>T	NCBI36
NG_011834.1:g.5249C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382357.4:c.-63+153C>T MANE Select	ENSP00000371794.3:n.-63+153C>T
ENST00000333337.3:c.-684C>T	ENSP00000331040.3:n.-684C>T
ENST00000382357.3:c.-63+153C>T	ENSP00000371794.3:n.-63+153C>T
ENST00000430860.1:c.-144C>T	ENSP00000391183.1:n.-144C>T
NM_005806.3:c.-63+153C>T	NP_005797.1:n.-63+153C>T
XM_005260908.1:c.-144C>T	XP_005260965.1:n.-144C>T
NM_005806.4:c.-63+153C>T MANE Select	NP_005797.1:n.-63+153C>T