Canonical Allele Identifier: CA1502380489

Gene: NR3C2

Linked Data

• dbSNP Id: rs1734144694
• gnomAD v4: 4-148152438-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152442del , CM000666.2:g.148152442del	GRCh38
NC_000004.11:g.149073593del , CM000666.1:g.149073593del	GRCh37
NC_000004.10:g.149293043del	NCBI36
NG_013350.1:g.295083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2510+30del MANE Select	ENSP00000350815.3:n.2510+30del
ENST00000342437.8:c.2015-32151del	ENSP00000343907.4:n.2015-32151del
ENST00000344721.8:c.2510+30del	ENSP00000341390.4:n.2510+30del
ENST00000358102.7:c.2510+30del	ENSP00000350815.3:n.2510+30del
ENST00000503174.1:n.469del
ENST00000503313.1:n.707+30del
ENST00000511528.1:c.2522+30del	ENSP00000421481.1:n.2522+30del
ENST00000512865.5:c.2159+30del	ENSP00000423510.1:n.2159+30del
ENST00000625323.2:c.2522+30del	ENSP00000486719.1:n.2522+30del
NM_000901.4:c.2510+30del	NP_000892.2:n.2510+30del
NM_001166104.1:c.2159+30del	NP_001159576.1:n.2159+30del
XM_011531975.1:c.2522+30del	XP_011530277.1:n.2522+30del
XM_011531976.1:c.2522+30del	XP_011530278.1:n.2522+30del
XM_011531977.1:c.2522+30del	XP_011530279.1:n.2522+30del
XM_011531978.1:c.2522+30del	XP_011530280.1:n.2522+30del
NM_001354819.1:c.2159+30del	NP_001341748.1:n.2159+30del
NR_148974.1:n.2378-32151del
XM_011531978.2:c.2522+30del	XP_011530280.1:n.2522+30del
NM_000901.5:c.2510+30del MANE Select	NP_000892.2:n.2510+30del
NM_001166104.2:c.2159+30del	NP_001159576.1:n.2159+30del
NR_148974.2:n.2272-32151del