Canonical Allele Identifier: CA1502380418
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152274C= , CM000666.2:g.148152274C= GRCh38
NC_000004.11:g.149073425C= , CM000666.1:g.149073425C= GRCh37
NC_000004.10:g.149292875C= NCBI36
NG_013350.1:g.295248G=

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.2510+195G= MANE Select ENSP00000350815.3:n.2510+195G=
ENST00000342437.8:c.2015-31986G= ENSP00000343907.4:n.2015-31986G=
ENST00000344721.8:c.2510+195G= ENSP00000341390.4:n.2510+195G=
ENST00000358102.7:c.2510+195G= ENSP00000350815.3:n.2510+195G=
ENST00000503313.1:n.707+195G=
ENST00000511528.1:c.2522+195G= ENSP00000421481.1:n.2522+195G=
ENST00000512865.5:c.2159+195G= ENSP00000423510.1:n.2159+195G=
ENST00000625323.2:c.2522+195G= ENSP00000486719.1:n.2522+195G=
NM_000901.4:c.2510+195G= NP_000892.2:n.2510+195G=
NM_001166104.1:c.2159+195G= NP_001159576.1:n.2159+195G=
XM_011531975.1:c.2522+195G= XP_011530277.1:n.2522+195G=
XM_011531976.1:c.2522+195G= XP_011530278.1:n.2522+195G=
XM_011531977.1:c.2522+195G= XP_011530279.1:n.2522+195G=
XM_011531978.1:c.2522+195G= XP_011530280.1:n.2522+195G=
NM_001354819.1:c.2159+195G= NP_001341748.1:n.2159+195G=
NR_148974.1:n.2378-31986G=
XM_011531978.2:c.2522+195G= XP_011530280.1:n.2522+195G=
NM_000901.5:c.2510+195G= MANE Select NP_000892.2:n.2510+195G=
NM_001166104.2:c.2159+195G= NP_001159576.1:n.2159+195G=
NR_148974.2:n.2272-31986G=