Canonical Allele Identifier: CA245386794

Gene: NCOR2

Linked Data

• dbSNP Id: rs1044339325
• MyVariant Identifiers: chr12:g.125033816C>G (hg19) ; chr12:g.124549270C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549270C>G , CM000674.2:g.124549270C>G	GRCh38
NC_000012.11:g.125033816C>G , CM000674.1:g.125033816C>G	GRCh37
NC_000012.10:g.123599769C>G	NCBI36
NG_022928.2:g.23195G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13659G>C MANE Select	ENSP00000384018.1:n.-164-13659G>C
ENST00000458234.5:c.-164-13659G>C	ENSP00000402808.1:n.-164-13659G>C
ENST00000542565.1:n.283-13659G>C
NM_001077261.3:c.-164-13659G>C	NP_001070729.2:n.-164-13659G>C
NM_001206654.1:c.-164-13659G>C	NP_001193583.1:n.-164-13659G>C
NM_006312.5:c.-164-13659G>C	NP_006303.4:n.-164-13659G>C
NM_001077261.4:c.-164-13659G>C	NP_001070729.2:n.-164-13659G>C
NM_001206654.2:c.-164-13659G>C	NP_001193583.1:n.-164-13659G>C
NM_006312.6:c.-164-13659G>C MANE Select	NP_006303.4:n.-164-13659G>C