Canonical Allele Identifier: CA748767215

Gene: OLIG2

Linked Data

• dbSNP Id: rs1384023312
• gnomAD v3: 21-33026163-GCT-G
• gnomAD v4: 21-33026163-GCT-G
• MyVariant Identifiers: chr21:g.34398472_34398473del (hg19) ; chr21:g.33026164_33026165del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33026166_33026167del , CM000683.2:g.33026166_33026167del	GRCh38
NC_000021.8:g.34398474_34398475del , CM000683.1:g.34398474_34398475del	GRCh37
NC_000021.7:g.33320344_33320345del	NCBI36
NG_011834.1:g.5236_5237del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382357.4:c.-63+140_-63+141del MANE Select	ENSP00000371794.3:n.-63+140_-63+141del
ENST00000333337.3:c.-697_-696del	ENSP00000331040.3:n.-697_-696del
ENST00000382357.3:c.-63+140_-63+141del	ENSP00000371794.3:n.-63+140_-63+141del
ENST00000430860.1:c.-157_-156del	ENSP00000391183.1:n.-157_-156del
NM_005806.3:c.-63+140_-63+141del	NP_005797.1:n.-63+140_-63+141del
XM_005260908.1:c.-157_-156del	XP_005260965.1:n.-157_-156del
NM_005806.4:c.-63+140_-63+141del MANE Select	NP_005797.1:n.-63+140_-63+141del