Canonical Allele Identifier: CA2069377566
Gene: NCOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124549320C= , CM000674.2:g.124549320C= GRCh38
NC_000012.11:g.125033866C= , CM000674.1:g.125033866C= GRCh37
NC_000012.10:g.123599819C= NCBI36
NG_022928.2:g.23145G=

Transcript Alleles

HGVS Amino-acid change
ENST00000405201.6:c.-164-13709G= MANE Select ENSP00000384018.1:n.-164-13709G=
ENST00000458234.5:c.-164-13709G= ENSP00000402808.1:n.-164-13709G=
ENST00000542565.1:n.283-13709G=
NM_001077261.3:c.-164-13709G= NP_001070729.2:n.-164-13709G=
NM_001206654.1:c.-164-13709G= NP_001193583.1:n.-164-13709G=
NM_006312.5:c.-164-13709G= NP_006303.4:n.-164-13709G=
NM_001077261.4:c.-164-13709G= NP_001070729.2:n.-164-13709G=
NM_001206654.2:c.-164-13709G= NP_001193583.1:n.-164-13709G=
NM_006312.6:c.-164-13709G= MANE Select NP_006303.4:n.-164-13709G=