Canonical Allele Identifier: CA2727386880

Gene: NCOR2

Linked Data

• dbSNP Id: rs2137251722

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549192T>A , CM000674.2:g.124549192T>A	GRCh38
NC_000012.11:g.125033738T>A , CM000674.1:g.125033738T>A	GRCh37
NC_000012.10:g.123599691T>A	NCBI36
NG_022928.2:g.23273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13581A>T MANE Select	ENSP00000384018.1:n.-164-13581A>T
ENST00000458234.5:c.-164-13581A>T	ENSP00000402808.1:n.-164-13581A>T
ENST00000542565.1:n.283-13581A>T
NM_001077261.3:c.-164-13581A>T	NP_001070729.2:n.-164-13581A>T
NM_001206654.1:c.-164-13581A>T	NP_001193583.1:n.-164-13581A>T
NM_006312.5:c.-164-13581A>T	NP_006303.4:n.-164-13581A>T
NM_001077261.4:c.-164-13581A>T	NP_001070729.2:n.-164-13581A>T
NM_001206654.2:c.-164-13581A>T	NP_001193583.1:n.-164-13581A>T
NM_006312.6:c.-164-13581A>T MANE Select	NP_006303.4:n.-164-13581A>T