Canonical Allele Identifier: CA1502331412
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148081368C= , CM000666.2:g.148081368C= GRCh38
NC_000004.11:g.149002519C= , CM000666.1:g.149002519C= GRCh37
NC_000004.10:g.149221969C= NCBI36
NG_013350.1:g.366154G=

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.2931G= MANE Select ENSP00000350815.3:p.Lys977=
ENST00000342437.8:c.*314G= ENSP00000343907.4:n.*314G=
ENST00000344721.8:c.2931G= ENSP00000341390.4:p.Lys977=
ENST00000358102.7:c.2931G= ENSP00000350815.3:p.Lys977=
ENST00000511528.1:c.2943G= ENSP00000421481.1:p.Lys981=
ENST00000512865.5:c.2580G= ENSP00000423510.1:p.Lys860=
ENST00000625323.2:c.2943G= ENSP00000486719.1:p.Lys981=
NM_000901.4:c.2931G= NP_000892.2:p.Lys977=
NM_001166104.1:c.2580G= NP_001159576.1:p.Lys860=
XM_011531975.1:c.2943G= XP_011530277.1:p.Lys981=
XM_011531976.1:c.2943G= XP_011530278.1:p.Lys981=
XM_011531977.1:c.2943G= XP_011530279.1:p.Lys981=
NM_001354819.1:c.2580G= NP_001341748.1:p.Lys860=
NR_148974.1:n.2798G=
NM_000901.5:c.2931G= MANE Select NP_000892.2:p.Lys977=
NM_001166104.2:c.2580G= NP_001159576.1:p.Lys860=
NR_148974.2:n.2692G=