Canonical Allele Identifier: CA1502333083
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148154803C= , CM000666.2:g.148154803C= GRCh38
NC_000004.11:g.149075954C= , CM000666.1:g.149075954C= GRCh37
NC_000004.10:g.149295404C= NCBI36
NG_013350.1:g.292719G=

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.2113G= MANE Select ENSP00000350815.3:p.Glu705=
ENST00000342437.8:c.2015-34515G= ENSP00000343907.4:n.2015-34515G=
ENST00000344721.8:c.2113G= ENSP00000341390.4:p.Glu705=
ENST00000358102.7:c.2113G= ENSP00000350815.3:p.Glu705=
ENST00000503174.1:n.42G=
ENST00000503313.1:n.310G=
ENST00000511528.1:c.2125G= ENSP00000421481.1:p.Glu709=
ENST00000512865.5:c.2015-2190G= ENSP00000423510.1:n.2015-2190G=
ENST00000625323.2:c.2125G= ENSP00000486719.1:p.Glu709=
NM_000901.4:c.2113G= NP_000892.2:p.Glu705=
NM_001166104.1:c.2015-2190G= NP_001159576.1:n.2015-2190G=
XM_011531975.1:c.2125G= XP_011530277.1:p.Glu709=
XM_011531976.1:c.2125G= XP_011530278.1:p.Glu709=
XM_011531977.1:c.2125G= XP_011530279.1:p.Glu709=
XM_011531978.1:c.2125G= XP_011530280.1:p.Glu709=
NM_001354819.1:c.2015-2190G= NP_001341748.1:n.2015-2190G=
NR_148974.1:n.2378-34515G=
XM_011531978.2:c.2125G= XP_011530280.1:p.Glu709=
NM_000901.5:c.2113G= MANE Select NP_000892.2:p.Glu705=
NM_001166104.2:c.2015-2190G= NP_001159576.1:n.2015-2190G=
NR_148974.2:n.2272-34515G=