Canonical Allele Identifier: CA1502380414
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152264G= , CM000666.2:g.148152264G= GRCh38
NC_000004.11:g.149073415G= , CM000666.1:g.149073415G= GRCh37
NC_000004.10:g.149292865G= NCBI36
NG_013350.1:g.295258C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2510+205C= MANE Select ENSP00000350815.3:n.2510+205C=
ENST00000342437.8:c.2015-31976C= ENSP00000343907.4:n.2015-31976C=
ENST00000344721.8:c.2510+205C= ENSP00000341390.4:n.2510+205C=
ENST00000358102.7:c.2510+205C= ENSP00000350815.3:n.2510+205C=
ENST00000503313.1:n.707+205C=
ENST00000511528.1:c.2522+205C= ENSP00000421481.1:n.2522+205C=
ENST00000512865.5:c.2159+205C= ENSP00000423510.1:n.2159+205C=
ENST00000625323.2:c.2522+205C= ENSP00000486719.1:n.2522+205C=
NM_000901.4:c.2510+205C= NP_000892.2:n.2510+205C=
NM_001166104.1:c.2159+205C= NP_001159576.1:n.2159+205C=
XM_011531975.1:c.2522+205C= XP_011530277.1:n.2522+205C=
XM_011531976.1:c.2522+205C= XP_011530278.1:n.2522+205C=
XM_011531977.1:c.2522+205C= XP_011530279.1:n.2522+205C=
XM_011531978.1:c.2522+205C= XP_011530280.1:n.2522+205C=
NM_001354819.1:c.2159+205C= NP_001341748.1:n.2159+205C=
NR_148974.1:n.2378-31976C=
XM_011531978.2:c.2522+205C= XP_011530280.1:n.2522+205C=
NM_000901.5:c.2510+205C= MANE Select NP_000892.2:n.2510+205C=
NM_001166104.2:c.2159+205C= NP_001159576.1:n.2159+205C=
NR_148974.2:n.2272-31976C=