Canonical Allele Identifier: CA952885522

Gene: NCOR2

Linked Data

• dbSNP Id: rs2051645863
• gnomAD v3: 12-124549508-GCA-G
• gnomAD v4: 12-124549508-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549511_124549512del , CM000674.2:g.124549511_124549512del	GRCh38
NC_000012.11:g.125034057_125034058del , CM000674.1:g.125034057_125034058del	GRCh37
NC_000012.10:g.123600010_123600011del	NCBI36
NG_022928.2:g.22955_22956del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13899_-164-13898del MANE Select	ENSP00000384018.1:n.-164-13899_-164-13898del
ENST00000458234.5:c.-164-13899_-164-13898del	ENSP00000402808.1:n.-164-13899_-164-13898del
ENST00000542565.1:n.283-13899_283-13898del
NM_001077261.3:c.-164-13899_-164-13898del	NP_001070729.2:n.-164-13899_-164-13898del
NM_001206654.1:c.-164-13899_-164-13898del	NP_001193583.1:n.-164-13899_-164-13898del
NM_006312.5:c.-164-13899_-164-13898del	NP_006303.4:n.-164-13899_-164-13898del
NM_001077261.4:c.-164-13899_-164-13898del	NP_001070729.2:n.-164-13899_-164-13898del
NM_001206654.2:c.-164-13899_-164-13898del	NP_001193583.1:n.-164-13899_-164-13898del
NM_006312.6:c.-164-13899_-164-13898del MANE Select	NP_006303.4:n.-164-13899_-164-13898del