Canonical Allele Identifier: CA1502380505
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152496T= , CM000666.2:g.148152496T= GRCh38
NC_000004.11:g.149073647T= , CM000666.1:g.149073647T= GRCh37
NC_000004.10:g.149293097T= NCBI36
NG_013350.1:g.295026A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2483A= MANE Select ENSP00000350815.3:p.Tyr828=
ENST00000342437.8:c.2015-32208A= ENSP00000343907.4:n.2015-32208A=
ENST00000344721.8:c.2483A= ENSP00000341390.4:p.Tyr828=
ENST00000358102.7:c.2483A= ENSP00000350815.3:p.Tyr828=
ENST00000503174.1:n.412A=
ENST00000503313.1:n.680A=
ENST00000511528.1:c.2495A= ENSP00000421481.1:p.Tyr832=
ENST00000512865.5:c.2132A= ENSP00000423510.1:p.Tyr711=
ENST00000625323.2:c.2495A= ENSP00000486719.1:p.Tyr832=
NM_000901.4:c.2483A= NP_000892.2:p.Tyr828=
NM_001166104.1:c.2132A= NP_001159576.1:p.Tyr711=
XM_011531975.1:c.2495A= XP_011530277.1:p.Tyr832=
XM_011531976.1:c.2495A= XP_011530278.1:p.Tyr832=
XM_011531977.1:c.2495A= XP_011530279.1:p.Tyr832=
XM_011531978.1:c.2495A= XP_011530280.1:p.Tyr832=
NM_001354819.1:c.2132A= NP_001341748.1:p.Tyr711=
NR_148974.1:n.2378-32208A=
XM_011531978.2:c.2495A= XP_011530280.1:p.Tyr832=
NM_000901.5:c.2483A= MANE Select NP_000892.2:p.Tyr828=
NM_001166104.2:c.2132A= NP_001159576.1:p.Tyr711=
NR_148974.2:n.2272-32208A=