Canonical Allele Identifier: CA13732328
Gene: NCOR2 HGNC NCBI

Linked Data

dbSNP Id: rs12423712

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124549387G>A , CM000674.2:g.124549387G>A GRCh38
NC_000012.11:g.125033933G>A , CM000674.1:g.125033933G>A GRCh37
NC_000012.10:g.123599886G>A NCBI36
NG_022928.2:g.23078C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000405201.6:c.-164-13776C>T MANE Select ENSP00000384018.1:n.-164-13776C>T
ENST00000458234.5:c.-164-13776C>T ENSP00000402808.1:n.-164-13776C>T
ENST00000542565.1:n.283-13776C>T
NM_001077261.3:c.-164-13776C>T NP_001070729.2:n.-164-13776C>T
NM_001206654.1:c.-164-13776C>T NP_001193583.1:n.-164-13776C>T
NM_006312.5:c.-164-13776C>T NP_006303.4:n.-164-13776C>T
NM_001077261.4:c.-164-13776C>T NP_001070729.2:n.-164-13776C>T
NM_001206654.2:c.-164-13776C>T NP_001193583.1:n.-164-13776C>T
NM_006312.6:c.-164-13776C>T MANE Select NP_006303.4:n.-164-13776C>T