Canonical Allele Identifier: CA788843161
Gene: NR3C2 HGNC NCBI

Linked Data

dbSNP Id: rs1462652304

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148280342_148280345del , CM000666.2:g.148280342_148280345del GRCh38
NC_000004.11:g.149201494_149201497del , CM000666.1:g.149201494_149201497del GRCh37
NC_000004.10:g.149420944_149420947del NCBI36
NG_013350.1:g.167179_167182del

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.1758-20225_1758-20222del MANE Select ENSP00000350815.3:n.1758-20225_1758-20222del
ENST00000342437.8:c.1758-20225_1758-20222del ENSP00000343907.4:n.1758-20225_1758-20222del
ENST00000344721.8:c.1758-20225_1758-20222del ENSP00000341390.4:n.1758-20225_1758-20222del
ENST00000358102.7:c.1758-20225_1758-20222del ENSP00000350815.3:n.1758-20225_1758-20222del
ENST00000504753.1:n.207-20225_207-20222del
ENST00000511528.1:c.1758-20225_1758-20222del ENSP00000421481.1:n.1758-20225_1758-20222del
ENST00000512865.5:c.1758-20225_1758-20222del ENSP00000423510.1:n.1758-20225_1758-20222del
ENST00000625323.2:c.1758-20225_1758-20222del ENSP00000486719.1:n.1758-20225_1758-20222del
NM_000901.4:c.1758-20225_1758-20222del NP_000892.2:n.1758-20225_1758-20222del
NM_001166104.1:c.1758-20225_1758-20222del NP_001159576.1:n.1758-20225_1758-20222del
XM_011531975.1:c.1758-20225_1758-20222del XP_011530277.1:n.1758-20225_1758-20222del
XM_011531976.1:c.1758-20225_1758-20222del XP_011530278.1:n.1758-20225_1758-20222del
XM_011531977.1:c.1758-20225_1758-20222del XP_011530279.1:n.1758-20225_1758-20222del
XM_011531978.1:c.1758-20225_1758-20222del XP_011530280.1:n.1758-20225_1758-20222del
NM_001354819.1:c.1758-20225_1758-20222del NP_001341748.1:n.1758-20225_1758-20222del
NR_148974.1:n.2121-20225_2121-20222del
XM_011531978.2:c.1758-20225_1758-20222del XP_011530280.1:n.1758-20225_1758-20222del
NM_000901.5:c.1758-20225_1758-20222del MANE Select NP_000892.2:n.1758-20225_1758-20222del
NM_001166104.2:c.1758-20225_1758-20222del NP_001159576.1:n.1758-20225_1758-20222del
NR_148974.2:n.2015-20225_2015-20222del