Canonical Allele Identifier: CA2069377669

Gene: NCOR2

Linked Data

• dbSNP Id: rs1594056427

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549513G>C , CM000674.2:g.124549513G>C	GRCh38
NC_000012.11:g.125034059G>C , CM000674.1:g.125034059G>C	GRCh37
NC_000012.10:g.123600012G>C	NCBI36
NG_022928.2:g.22952C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13902C>G MANE Select	ENSP00000384018.1:n.-164-13902C>G
ENST00000458234.5:c.-164-13902C>G	ENSP00000402808.1:n.-164-13902C>G
ENST00000542565.1:n.283-13902C>G
NM_001077261.3:c.-164-13902C>G	NP_001070729.2:n.-164-13902C>G
NM_001206654.1:c.-164-13902C>G	NP_001193583.1:n.-164-13902C>G
NM_006312.5:c.-164-13902C>G	NP_006303.4:n.-164-13902C>G
NM_001077261.4:c.-164-13902C>G	NP_001070729.2:n.-164-13902C>G
NM_001206654.2:c.-164-13902C>G	NP_001193583.1:n.-164-13902C>G
NM_006312.6:c.-164-13902C>G MANE Select	NP_006303.4:n.-164-13902C>G