Canonical Allele Identifier: CA608284400

Gene: NCOR2

Linked Data

• dbSNP Id: rs1192777451
• gnomAD v2: 12-125033774-GGCATGT-G
• gnomAD v3: 12-124549228-GGCATGT-G
• gnomAD v4: 12-124549228-GGCATGT-G
• MyVariant Identifiers: chr12:g.125033775_125033780del (hg19) ; chr12:g.124549229_124549234del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549231_124549236del , CM000674.2:g.124549231_124549236del	GRCh38
NC_000012.11:g.125033777_125033782del , CM000674.1:g.125033777_125033782del	GRCh37
NC_000012.10:g.123599730_123599735del	NCBI36
NG_022928.2:g.23231_23236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13623_-164-13618del MANE Select	ENSP00000384018.1:n.-164-13623_-164-13618del
ENST00000458234.5:c.-164-13623_-164-13618del	ENSP00000402808.1:n.-164-13623_-164-13618del
ENST00000542565.1:n.283-13623_283-13618del
NM_001077261.3:c.-164-13623_-164-13618del	NP_001070729.2:n.-164-13623_-164-13618del
NM_001206654.1:c.-164-13623_-164-13618del	NP_001193583.1:n.-164-13623_-164-13618del
NM_006312.5:c.-164-13623_-164-13618del	NP_006303.4:n.-164-13623_-164-13618del
NM_001077261.4:c.-164-13623_-164-13618del	NP_001070729.2:n.-164-13623_-164-13618del
NM_001206654.2:c.-164-13623_-164-13618del	NP_001193583.1:n.-164-13623_-164-13618del
NM_006312.6:c.-164-13623_-164-13618del MANE Select	NP_006303.4:n.-164-13623_-164-13618del