Canonical Allele Identifier: CA684779670

Gene: NCOR2

Linked Data

• dbSNP Id: rs1379403066
• gnomAD v3: 12-124549496-C-T
• gnomAD v4: 12-124549496-C-T
• MyVariant Identifiers: chr12:g.125034042C>T (hg19) ; chr12:g.124549496C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124549496C>T , CM000674.2:g.124549496C>T	GRCh38
NC_000012.11:g.125034042C>T , CM000674.1:g.125034042C>T	GRCh37
NC_000012.10:g.123599995C>T	NCBI36
NG_022928.2:g.22969G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.-164-13885G>A MANE Select	ENSP00000384018.1:n.-164-13885G>A
ENST00000458234.5:c.-164-13885G>A	ENSP00000402808.1:n.-164-13885G>A
ENST00000542565.1:n.283-13885G>A
NM_001077261.3:c.-164-13885G>A	NP_001070729.2:n.-164-13885G>A
NM_001206654.1:c.-164-13885G>A	NP_001193583.1:n.-164-13885G>A
NM_006312.5:c.-164-13885G>A	NP_006303.4:n.-164-13885G>A
NM_001077261.4:c.-164-13885G>A	NP_001070729.2:n.-164-13885G>A
NM_001206654.2:c.-164-13885G>A	NP_001193583.1:n.-164-13885G>A
NM_006312.6:c.-164-13885G>A MANE Select	NP_006303.4:n.-164-13885G>A