Canonical Allele Identifier: CA2069377528

Gene: NCOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549238G= , CM000674.2:g.124549238G=	GRCh38
NC_000012.11:g.125033784G= , CM000674.1:g.125033784G=	GRCh37
NC_000012.10:g.123599737G=	NCBI36
NG_022928.2:g.23227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13627C= MANE Select	ENSP00000384018.1:n.-164-13627C=
ENST00000458234.5:c.-164-13627C=	ENSP00000402808.1:n.-164-13627C=
ENST00000542565.1:n.283-13627C=
NM_001077261.3:c.-164-13627C=	NP_001070729.2:n.-164-13627C=
NM_001206654.1:c.-164-13627C=	NP_001193583.1:n.-164-13627C=
NM_006312.5:c.-164-13627C=	NP_006303.4:n.-164-13627C=
NM_001077261.4:c.-164-13627C=	NP_001070729.2:n.-164-13627C=
NM_001206654.2:c.-164-13627C=	NP_001193583.1:n.-164-13627C=
NM_006312.6:c.-164-13627C= MANE Select	NP_006303.4:n.-164-13627C=