Canonical Allele Identifier: CA1502416397
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148299870A= , CM000666.2:g.148299870A= GRCh38
NC_000004.11:g.149221022A= , CM000666.1:g.149221022A= GRCh37
NC_000004.10:g.149440472A= NCBI36
NG_013350.1:g.147651T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.1758-39753T= MANE Select ENSP00000350815.3:n.1758-39753T=
ENST00000342437.8:c.1758-39753T= ENSP00000343907.4:n.1758-39753T=
ENST00000344721.8:c.1758-39753T= ENSP00000341390.4:n.1758-39753T=
ENST00000358102.7:c.1758-39753T= ENSP00000350815.3:n.1758-39753T=
ENST00000504753.1:n.207-39753T=
ENST00000511528.1:c.1758-39753T= ENSP00000421481.1:n.1758-39753T=
ENST00000512865.5:c.1758-39753T= ENSP00000423510.1:n.1758-39753T=
ENST00000625323.2:c.1758-39753T= ENSP00000486719.1:n.1758-39753T=
NM_000901.4:c.1758-39753T= NP_000892.2:n.1758-39753T=
NM_001166104.1:c.1758-39753T= NP_001159576.1:n.1758-39753T=
XM_011531975.1:c.1758-39753T= XP_011530277.1:n.1758-39753T=
XM_011531976.1:c.1758-39753T= XP_011530278.1:n.1758-39753T=
XM_011531977.1:c.1758-39753T= XP_011530279.1:n.1758-39753T=
XM_011531978.1:c.1758-39753T= XP_011530280.1:n.1758-39753T=
NM_001354819.1:c.1758-39753T= NP_001341748.1:n.1758-39753T=
NR_148974.1:n.2121-39753T=
XM_011531978.2:c.1758-39753T= XP_011530280.1:n.1758-39753T=
NM_000901.5:c.1758-39753T= MANE Select NP_000892.2:n.1758-39753T=
NM_001166104.2:c.1758-39753T= NP_001159576.1:n.1758-39753T=
NR_148974.2:n.2015-39753T=