Canonical Allele Identifier: CA1502333557

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154881C= , CM000666.2:g.148154881C=	GRCh38
NC_000004.11:g.149076032C= , CM000666.1:g.149076032C=	GRCh37
NC_000004.10:g.149295482C=	NCBI36
NG_013350.1:g.292641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2035G= MANE Select	ENSP00000350815.3:p.Gly679=
ENST00000342437.8:c.2015-34593G=	ENSP00000343907.4:n.2015-34593G=
ENST00000344721.8:c.2035G=	ENSP00000341390.4:p.Gly679=
ENST00000358102.7:c.2035G=	ENSP00000350815.3:p.Gly679=
ENST00000503313.1:n.232G=
ENST00000511528.1:c.2047G=	ENSP00000421481.1:p.Gly683=
ENST00000512865.5:c.2015-2268G=	ENSP00000423510.1:n.2015-2268G=
ENST00000625323.2:c.2047G=	ENSP00000486719.1:p.Gly683=
NM_000901.4:c.2035G=	NP_000892.2:p.Gly679=
NM_001166104.1:c.2015-2268G=	NP_001159576.1:n.2015-2268G=
XM_011531975.1:c.2047G=	XP_011530277.1:p.Gly683=
XM_011531976.1:c.2047G=	XP_011530278.1:p.Gly683=
XM_011531977.1:c.2047G=	XP_011530279.1:p.Gly683=
XM_011531978.1:c.2047G=	XP_011530280.1:p.Gly683=
NM_001354819.1:c.2015-2268G=	NP_001341748.1:n.2015-2268G=
NR_148974.1:n.2378-34593G=
XM_011531978.2:c.2047G=	XP_011530280.1:p.Gly683=
NM_000901.5:c.2035G= MANE Select	NP_000892.2:p.Gly679=
NM_001166104.2:c.2015-2268G=	NP_001159576.1:n.2015-2268G=
NR_148974.2:n.2272-34593G=