Canonical Allele Identifier: CA788844190

Gene: NR3C2

Linked Data

• dbSNP Id: rs1236683026
• gnomAD v3: 4-148126910-G-GT
• gnomAD v4: 4-148126910-G-GT
• MyVariant Identifiers: chr4:g.149048061_149048062insT (hg19) ; chr4:g.148126910_148126911insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148126916dup , CM000666.2:g.148126916dup	GRCh38
NC_000004.11:g.149048067dup , CM000666.1:g.149048067dup	GRCh37
NC_000004.10:g.149267517dup	NCBI36
NG_013350.1:g.320611dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2511-6623dup MANE Select	ENSP00000350815.3:n.2511-6623dup
ENST00000342437.8:c.2015-6623dup	ENSP00000343907.4:n.2015-6623dup
ENST00000344721.8:c.2511-6623dup	ENSP00000341390.4:n.2511-6623dup
ENST00000358102.7:c.2511-6623dup	ENSP00000350815.3:n.2511-6623dup
ENST00000511528.1:c.2523-6623dup	ENSP00000421481.1:n.2523-6623dup
ENST00000512865.5:c.2160-6623dup	ENSP00000423510.1:n.2160-6623dup
ENST00000625323.2:c.2523-6623dup	ENSP00000486719.1:n.2523-6623dup
NM_000901.4:c.2511-6623dup	NP_000892.2:n.2511-6623dup
NM_001166104.1:c.2160-6623dup	NP_001159576.1:n.2160-6623dup
XM_011531975.1:c.2523-6623dup	XP_011530277.1:n.2523-6623dup
XM_011531976.1:c.2523-6623dup	XP_011530278.1:n.2523-6623dup
XM_011531977.1:c.2523-6623dup	XP_011530279.1:n.2523-6623dup
NM_001354819.1:c.2160-6623dup	NP_001341748.1:n.2160-6623dup
NR_148974.1:n.2378-6623dup
NM_000901.5:c.2511-6623dup MANE Select	NP_000892.2:n.2511-6623dup
NM_001166104.2:c.2160-6623dup	NP_001159576.1:n.2160-6623dup
NR_148974.2:n.2272-6623dup