Canonical Allele Identifier: CA1502460420

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148436760G= , CM000666.2:g.148436760G=	GRCh38
NC_000004.11:g.149357912G= , CM000666.1:g.149357912G=	GRCh37
NC_000004.10:g.149577362G=	NCBI36
NG_013350.1:g.10761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.101C= MANE Select	ENSP00000350815.3:p.Thr34=
ENST00000342437.8:c.101C=	ENSP00000343907.4:p.Thr34=
ENST00000344721.8:c.101C=	ENSP00000341390.4:p.Thr34=
ENST00000358102.7:c.101C=	ENSP00000350815.3:p.Thr34=
ENST00000511528.1:c.101C=	ENSP00000421481.1:p.Thr34=
ENST00000512865.5:c.101C=	ENSP00000423510.1:p.Thr34=
ENST00000625323.2:c.101C=	ENSP00000486719.1:p.Thr34=
NM_000901.4:c.101C=	NP_000892.2:p.Thr34=
NM_001166104.1:c.101C=	NP_001159576.1:p.Thr34=
XM_011531975.1:c.101C=	XP_011530277.1:p.Thr34=
XM_011531976.1:c.101C=	XP_011530278.1:p.Thr34=
XM_011531977.1:c.101C=	XP_011530279.1:p.Thr34=
XM_011531978.1:c.101C=	XP_011530280.1:p.Thr34=
NM_001354819.1:c.101C=	NP_001341748.1:p.Thr34=
NR_148974.1:n.464C=
XM_011531978.2:c.101C=	XP_011530280.1:p.Thr34=
NM_000901.5:c.101C= MANE Select	NP_000892.2:p.Thr34=
NM_001166104.2:c.101C=	NP_001159576.1:p.Thr34=
NR_148974.2:n.358C=