Canonical Allele Identifier: CA684779497
Gene: NCOR2 HGNC NCBI

Linked Data

dbSNP Id: rs1443049284
gnomAD v3: 12-124549138-A-T
gnomAD v4: 12-124549138-A-T
MyVariant Identifiers: chr12:g.125033684A>T (hg19) chr12:g.124549138A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124549138A>T , CM000674.2:g.124549138A>T GRCh38
NC_000012.11:g.125033684A>T , CM000674.1:g.125033684A>T GRCh37
NC_000012.10:g.123599637A>T NCBI36
NG_022928.2:g.23327T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405201.6:c.-164-13527T>A MANE Select ENSP00000384018.1:n.-164-13527T>A
ENST00000458234.5:c.-164-13527T>A ENSP00000402808.1:n.-164-13527T>A
ENST00000542565.1:n.283-13527T>A
NM_001077261.3:c.-164-13527T>A NP_001070729.2:n.-164-13527T>A
NM_001206654.1:c.-164-13527T>A NP_001193583.1:n.-164-13527T>A
NM_006312.5:c.-164-13527T>A NP_006303.4:n.-164-13527T>A
NM_001077261.4:c.-164-13527T>A NP_001070729.2:n.-164-13527T>A
NM_001206654.2:c.-164-13527T>A NP_001193583.1:n.-164-13527T>A
NM_006312.6:c.-164-13527T>A MANE Select NP_006303.4:n.-164-13527T>A
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