Canonical Allele Identifier: CA1502380519
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152531C= , CM000666.2:g.148152531C= GRCh38
NC_000004.11:g.149073682C= , CM000666.1:g.149073682C= GRCh37
NC_000004.10:g.149293132C= NCBI36
NG_013350.1:g.294991G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2448G= MANE Select ENSP00000350815.3:p.Trp816=
ENST00000342437.8:c.2015-32243G= ENSP00000343907.4:n.2015-32243G=
ENST00000344721.8:c.2448G= ENSP00000341390.4:p.Trp816=
ENST00000358102.7:c.2448G= ENSP00000350815.3:p.Trp816=
ENST00000503174.1:n.377G=
ENST00000503313.1:n.645G=
ENST00000511528.1:c.2460G= ENSP00000421481.1:p.Trp820=
ENST00000512865.5:c.2097G= ENSP00000423510.1:p.Trp699=
ENST00000625323.2:c.2460G= ENSP00000486719.1:p.Trp820=
NM_000901.4:c.2448G= NP_000892.2:p.Trp816=
NM_001166104.1:c.2097G= NP_001159576.1:p.Trp699=
XM_011531975.1:c.2460G= XP_011530277.1:p.Trp820=
XM_011531976.1:c.2460G= XP_011530278.1:p.Trp820=
XM_011531977.1:c.2460G= XP_011530279.1:p.Trp820=
XM_011531978.1:c.2460G= XP_011530280.1:p.Trp820=
NM_001354819.1:c.2097G= NP_001341748.1:p.Trp699=
NR_148974.1:n.2378-32243G=
XM_011531978.2:c.2460G= XP_011530280.1:p.Trp820=
NM_000901.5:c.2448G= MANE Select NP_000892.2:p.Trp816=
NM_001166104.2:c.2097G= NP_001159576.1:p.Trp699=
NR_148974.2:n.2272-32243G=