Canonical Allele Identifier: CA245386802
Gene: NCOR2 HGNC NCBI

Linked Data

dbSNP Id: rs11057667
gnomAD v2: 12-125033839-G-T
gnomAD v3: 12-124549293-G-T
gnomAD v4: 12-124549293-G-T
MyVariant Identifiers: chr12:g.125033839G>T (hg19) chr12:g.124549293G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124549293G>T , CM000674.2:g.124549293G>T GRCh38
NC_000012.11:g.125033839G>T , CM000674.1:g.125033839G>T GRCh37
NC_000012.10:g.123599792G>T NCBI36
NG_022928.2:g.23172C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405201.6:c.-164-13682C>A MANE Select ENSP00000384018.1:n.-164-13682C>A
ENST00000458234.5:c.-164-13682C>A ENSP00000402808.1:n.-164-13682C>A
ENST00000542565.1:n.283-13682C>A
NM_001077261.3:c.-164-13682C>A NP_001070729.2:n.-164-13682C>A
NM_001206654.1:c.-164-13682C>A NP_001193583.1:n.-164-13682C>A
NM_006312.5:c.-164-13682C>A NP_006303.4:n.-164-13682C>A
NM_001077261.4:c.-164-13682C>A NP_001070729.2:n.-164-13682C>A
NM_001206654.2:c.-164-13682C>A NP_001193583.1:n.-164-13682C>A
NM_006312.6:c.-164-13682C>A MANE Select NP_006303.4:n.-164-13682C>A
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