Canonical Allele Identifier: CA245386839

Gene: NCOR2

Linked Data

• dbSNP Id: rs373812620
• gnomAD v2: 12-125033932-C-G
• gnomAD v3: 12-124549386-C-G
• gnomAD v4: 12-124549386-C-G
• MyVariant Identifiers: chr12:g.125033932C>G (hg19) ; chr12:g.124549386C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549386C>G , CM000674.2:g.124549386C>G	GRCh38
NC_000012.11:g.125033932C>G , CM000674.1:g.125033932C>G	GRCh37
NC_000012.10:g.123599885C>G	NCBI36
NG_022928.2:g.23079G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13775G>C MANE Select	ENSP00000384018.1:n.-164-13775G>C
ENST00000458234.5:c.-164-13775G>C	ENSP00000402808.1:n.-164-13775G>C
ENST00000542565.1:n.283-13775G>C
NM_001077261.3:c.-164-13775G>C	NP_001070729.2:n.-164-13775G>C
NM_001206654.1:c.-164-13775G>C	NP_001193583.1:n.-164-13775G>C
NM_006312.5:c.-164-13775G>C	NP_006303.4:n.-164-13775G>C
NM_001077261.4:c.-164-13775G>C	NP_001070729.2:n.-164-13775G>C
NM_001206654.2:c.-164-13775G>C	NP_001193583.1:n.-164-13775G>C
NM_006312.6:c.-164-13775G>C MANE Select	NP_006303.4:n.-164-13775G>C