Canonical Allele Identifier: CA3100210
Gene: NR3C2 HGNC NCBI

Linked Data

dbSNP Id: rs774732922

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148194892_148194896del , CM000666.2:g.148194892_148194896del GRCh38
NC_000004.11:g.149116043_149116047del , CM000666.1:g.149116043_149116047del GRCh37
NC_000004.10:g.149335493_149335497del NCBI36
NG_013350.1:g.252628_252632del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.1898-32_1898-28del MANE Select ENSP00000350815.3:n.1898-32_1898-28del
ENST00000342437.8:c.1898-32_1898-28del ENSP00000343907.4:n.1898-32_1898-28del
ENST00000344721.8:c.1898-32_1898-28del ENSP00000341390.4:n.1898-32_1898-28del
ENST00000358102.7:c.1898-32_1898-28del ENSP00000350815.3:n.1898-32_1898-28del
ENST00000503313.1:n.95-32_95-28del
ENST00000504753.1:n.347-32_347-28del
ENST00000511528.1:c.1910-32_1910-28del ENSP00000421481.1:n.1910-32_1910-28del
ENST00000512865.5:c.1898-32_1898-28del ENSP00000423510.1:n.1898-32_1898-28del
ENST00000625323.2:c.1910-32_1910-28del ENSP00000486719.1:n.1910-32_1910-28del
NM_000901.4:c.1898-32_1898-28del NP_000892.2:n.1898-32_1898-28del
NM_001166104.1:c.1898-32_1898-28del NP_001159576.1:n.1898-32_1898-28del
XM_011531975.1:c.1910-32_1910-28del XP_011530277.1:n.1910-32_1910-28del
XM_011531976.1:c.1910-32_1910-28del XP_011530278.1:n.1910-32_1910-28del
XM_011531977.1:c.1910-32_1910-28del XP_011530279.1:n.1910-32_1910-28del
XM_011531978.1:c.1910-32_1910-28del XP_011530280.1:n.1910-32_1910-28del
NM_001354819.1:c.1898-32_1898-28del NP_001341748.1:n.1898-32_1898-28del
NR_148974.1:n.2261-32_2261-28del
XM_011531978.2:c.1910-32_1910-28del XP_011530280.1:n.1910-32_1910-28del
NM_000901.5:c.1898-32_1898-28del MANE Select NP_000892.2:n.1898-32_1898-28del
NM_001166104.2:c.1898-32_1898-28del NP_001159576.1:n.1898-32_1898-28del
NR_148974.2:n.2155-32_2155-28del