Canonical Allele Identifier: CA2069377659

Gene: NCOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549497C= , CM000674.2:g.124549497C=	GRCh38
NC_000012.11:g.125034043C= , CM000674.1:g.125034043C=	GRCh37
NC_000012.10:g.123599996C=	NCBI36
NG_022928.2:g.22968G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13886G= MANE Select	ENSP00000384018.1:n.-164-13886G=
ENST00000458234.5:c.-164-13886G=	ENSP00000402808.1:n.-164-13886G=
ENST00000542565.1:n.283-13886G=
NM_001077261.3:c.-164-13886G=	NP_001070729.2:n.-164-13886G=
NM_001206654.1:c.-164-13886G=	NP_001193583.1:n.-164-13886G=
NM_006312.5:c.-164-13886G=	NP_006303.4:n.-164-13886G=
NM_001077261.4:c.-164-13886G=	NP_001070729.2:n.-164-13886G=
NM_001206654.2:c.-164-13886G=	NP_001193583.1:n.-164-13886G=
NM_006312.6:c.-164-13886G= MANE Select	NP_006303.4:n.-164-13886G=