Canonical Allele Identifier: CA387209236

Gene: NCOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124336959G>T , CM000674.2:g.124336959G>T	GRCh38
NC_000012.11:g.124821505G>T , CM000674.1:g.124821505G>T	GRCh37
NC_000012.10:g.123387458G>T	NCBI36
NG_022928.2:g.235506C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006312.6:c.5909C>A MANE Select	NP_006303.4:p.Ser1970Tyr
ENST00000405201.6:c.5909C>A MANE Select	ENSP00000384018.1:p.Ser1970Tyr
NM_001077261.3:c.5879C>A	NP_001070729.2:p.Ser1960Tyr
NM_001077261.4:c.5879C>A	NP_001070729.2:p.Ser1960Tyr
NM_001206654.1:c.5879C>A	NP_001193583.1:p.Ser1960Tyr
NM_001206654.2:c.5879C>A	NP_001193583.1:p.Ser1960Tyr
NM_006312.5:c.5909C>A	NP_006303.4:p.Ser1970Tyr
ENST00000356219.7:c.4604C>A	ENSP00000348551.4:p.Ser1535Tyr
ENST00000404121.6:c.4553C>A	ENSP00000385618.3:p.Ser1518Tyr
ENST00000404621.5:c.5879C>A	ENSP00000384202.1:p.Ser1960Tyr
ENST00000405201.5:c.5909C>A	ENSP00000384018.1:p.Ser1970Tyr
ENST00000429285.6:c.5879C>A	ENSP00000400281.2:p.Ser1960Tyr