Canonical Allele Identifier: CA1069288452

Gene: NR3C2

Linked Data

• dbSNP Id: rs1734154840
• gnomAD v3: 4-148152635-C-T
• gnomAD v4: 4-148152635-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152635C>T , CM000666.2:g.148152635C>T	GRCh38
NC_000004.11:g.149073786C>T , CM000666.1:g.149073786C>T	GRCh37
NC_000004.10:g.149293236C>T	NCBI36
NG_013350.1:g.294887G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2366-22G>A MANE Select	ENSP00000350815.3:n.2366-22G>A
ENST00000342437.8:c.2015-32347G>A	ENSP00000343907.4:n.2015-32347G>A
ENST00000344721.8:c.2366-22G>A	ENSP00000341390.4:n.2366-22G>A
ENST00000358102.7:c.2366-22G>A	ENSP00000350815.3:n.2366-22G>A
ENST00000503174.1:n.295-22G>A
ENST00000503313.1:n.563-22G>A
ENST00000511528.1:c.2378-22G>A	ENSP00000421481.1:n.2378-22G>A
ENST00000512865.5:c.2015-22G>A	ENSP00000423510.1:n.2015-22G>A
ENST00000625323.2:c.2378-22G>A	ENSP00000486719.1:n.2378-22G>A
NM_000901.4:c.2366-22G>A	NP_000892.2:n.2366-22G>A
NM_001166104.1:c.2015-22G>A	NP_001159576.1:n.2015-22G>A
XM_011531975.1:c.2378-22G>A	XP_011530277.1:n.2378-22G>A
XM_011531976.1:c.2378-22G>A	XP_011530278.1:n.2378-22G>A
XM_011531977.1:c.2378-22G>A	XP_011530279.1:n.2378-22G>A
XM_011531978.1:c.2378-22G>A	XP_011530280.1:n.2378-22G>A
NM_001354819.1:c.2015-22G>A	NP_001341748.1:n.2015-22G>A
NR_148974.1:n.2378-32347G>A
XM_011531978.2:c.2378-22G>A	XP_011530280.1:n.2378-22G>A
NM_000901.5:c.2366-22G>A MANE Select	NP_000892.2:n.2366-22G>A
NM_001166104.2:c.2015-22G>A	NP_001159576.1:n.2015-22G>A
NR_148974.2:n.2272-32347G>A