Canonical Allele Identifier: CA107877748

Gene: NR3C2

Linked Data

• dbSNP Id: rs897625794
• gnomAD v4: 4-148442411-A-AGAGGAG
• MyVariant Identifiers: chr4:g.149363563_149363564insGAGGAG (hg19) ; chr4:g.148442411_148442412insGAGGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442413_148442418dup , CM000666.2:g.148442413_148442418dup	GRCh38
NC_000004.11:g.149363565_149363570dup , CM000666.1:g.149363565_149363570dup	GRCh37
NC_000004.10:g.149583015_149583020dup	NCBI36
NG_013350.1:g.5104_5109dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344721.8:c.-3+2109_-3+2114dup	ENSP00000341390.4:n.-3+2109_-3+2114dup
ENST00000358102.7:c.-260_-255dup	ENSP00000350815.3:n.-260_-255dup
ENST00000625323.2:c.-260_-255dup	ENSP00000486719.1:n.-260_-255dup
NM_000901.4:c.-260_-255dup	NP_000892.2:n.-260_-255dup
NM_001166104.1:c.-260_-255dup	NP_001159576.1:n.-260_-255dup
XM_011531975.1:c.-260_-255dup	XP_011530277.1:n.-260_-255dup
XM_011531976.1:c.-3+2109_-3+2114dup	XP_011530278.1:n.-3+2109_-3+2114dup
XM_011531977.1:c.-3+2783_-3+2788dup	XP_011530279.1:n.-3+2783_-3+2788dup
XM_011531978.1:c.-260_-255dup	XP_011530280.1:n.-260_-255dup
NM_001354819.1:c.-3+2109_-3+2114dup	NP_001341748.1:n.-3+2109_-3+2114dup
NR_148974.1:n.104_109dup
XM_011531978.2:c.-260_-255dup	XP_011530280.1:n.-260_-255dup