Canonical Allele Identifier: CA1502381464

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154524A= , CM000666.2:g.148154524A=	GRCh38
NC_000004.11:g.149075675A= , CM000666.1:g.149075675A=	GRCh37
NC_000004.10:g.149295125A=	NCBI36
NG_013350.1:g.292998T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2365+27T= MANE Select	ENSP00000350815.3:n.2365+27T=
ENST00000342437.8:c.2015-34236T=	ENSP00000343907.4:n.2015-34236T=
ENST00000344721.8:c.2365+27T=	ENSP00000341390.4:n.2365+27T=
ENST00000358102.7:c.2365+27T=	ENSP00000350815.3:n.2365+27T=
ENST00000503174.1:n.294+27T=
ENST00000503313.1:n.562+27T=
ENST00000511528.1:c.2377+27T=	ENSP00000421481.1:n.2377+27T=
ENST00000512865.5:c.2015-1911T=	ENSP00000423510.1:n.2015-1911T=
ENST00000625323.2:c.2377+27T=	ENSP00000486719.1:n.2377+27T=
NM_000901.4:c.2365+27T=	NP_000892.2:n.2365+27T=
NM_001166104.1:c.2015-1911T=	NP_001159576.1:n.2015-1911T=
XM_011531975.1:c.2377+27T=	XP_011530277.1:n.2377+27T=
XM_011531976.1:c.2377+27T=	XP_011530278.1:n.2377+27T=
XM_011531977.1:c.2377+27T=	XP_011530279.1:n.2377+27T=
XM_011531978.1:c.2377+27T=	XP_011530280.1:n.2377+27T=
NM_001354819.1:c.2015-1911T=	NP_001341748.1:n.2015-1911T=
NR_148974.1:n.2378-34236T=
XM_011531978.2:c.2377+27T=	XP_011530280.1:n.2377+27T=
NM_000901.5:c.2365+27T= MANE Select	NP_000892.2:n.2365+27T=
NM_001166104.2:c.2015-1911T=	NP_001159576.1:n.2015-1911T=
NR_148974.2:n.2272-34236T=