Canonical Allele Identifier: CA1502414647
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148194825G= , CM000666.2:g.148194825G= GRCh38
NC_000004.11:g.149115976G= , CM000666.1:g.149115976G= GRCh37
NC_000004.10:g.149335426G= NCBI36
NG_013350.1:g.252697C=

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.1935C= MANE Select ENSP00000350815.3:p.Cys645=
ENST00000342437.8:c.1935C= ENSP00000343907.4:p.Cys645=
ENST00000344721.8:c.1935C= ENSP00000341390.4:p.Cys645=
ENST00000358102.7:c.1935C= ENSP00000350815.3:p.Cys645=
ENST00000503313.1:n.132C=
ENST00000504753.1:n.384C=
ENST00000511528.1:c.1947C= ENSP00000421481.1:p.Cys649=
ENST00000512865.5:c.1935C= ENSP00000423510.1:p.Cys645=
ENST00000625323.2:c.1947C= ENSP00000486719.1:p.Cys649=
NM_000901.4:c.1935C= NP_000892.2:p.Cys645=
NM_001166104.1:c.1935C= NP_001159576.1:p.Cys645=
XM_011531975.1:c.1947C= XP_011530277.1:p.Cys649=
XM_011531976.1:c.1947C= XP_011530278.1:p.Cys649=
XM_011531977.1:c.1947C= XP_011530279.1:p.Cys649=
XM_011531978.1:c.1947C= XP_011530280.1:p.Cys649=
NM_001354819.1:c.1935C= NP_001341748.1:p.Cys645=
NR_148974.1:n.2298C=
XM_011531978.2:c.1947C= XP_011530280.1:p.Cys649=
NM_000901.5:c.1935C= MANE Select NP_000892.2:p.Cys645=
NM_001166104.2:c.1935C= NP_001159576.1:p.Cys645=
NR_148974.2:n.2192C=