Canonical Allele Identifier: CA2672313825

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148152392-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152392G>T , CM000666.2:g.148152392G>T	GRCh38
NC_000004.11:g.149073543G>T , CM000666.1:g.149073543G>T	GRCh37
NC_000004.10:g.149292993G>T	NCBI36
NG_013350.1:g.295130C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2510+77C>A MANE Select	ENSP00000350815.3:n.2510+77C>A
ENST00000342437.8:c.2015-32104C>A	ENSP00000343907.4:n.2015-32104C>A
ENST00000344721.8:c.2510+77C>A	ENSP00000341390.4:n.2510+77C>A
ENST00000358102.7:c.2510+77C>A	ENSP00000350815.3:n.2510+77C>A
ENST00000503313.1:n.707+77C>A
ENST00000511528.1:c.2522+77C>A	ENSP00000421481.1:n.2522+77C>A
ENST00000512865.5:c.2159+77C>A	ENSP00000423510.1:n.2159+77C>A
ENST00000625323.2:c.2522+77C>A	ENSP00000486719.1:n.2522+77C>A
NM_000901.4:c.2510+77C>A	NP_000892.2:n.2510+77C>A
NM_001166104.1:c.2159+77C>A	NP_001159576.1:n.2159+77C>A
XM_011531975.1:c.2522+77C>A	XP_011530277.1:n.2522+77C>A
XM_011531976.1:c.2522+77C>A	XP_011530278.1:n.2522+77C>A
XM_011531977.1:c.2522+77C>A	XP_011530279.1:n.2522+77C>A
XM_011531978.1:c.2522+77C>A	XP_011530280.1:n.2522+77C>A
NM_001354819.1:c.2159+77C>A	NP_001341748.1:n.2159+77C>A
NR_148974.1:n.2378-32104C>A
XM_011531978.2:c.2522+77C>A	XP_011530280.1:n.2522+77C>A
NM_000901.5:c.2510+77C>A MANE Select	NP_000892.2:n.2510+77C>A
NM_001166104.2:c.2159+77C>A	NP_001159576.1:n.2159+77C>A
NR_148974.2:n.2272-32104C>A