Canonical Allele Identifier: CA1082411666

Gene: NR3C1

Linked Data

• dbSNP Id: rs1751528464
• gnomAD v3: 5-143426345-A-AT
• gnomAD v4: 5-143426345-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426347dup , CM000667.2:g.143426347dup	GRCh38
NC_000005.9:g.142805912dup , CM000667.1:g.142805912dup	GRCh37
NC_000005.8:g.142786105dup	NCBI36
NG_009062.1:g.14167dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8186dup	ENSP00000343205.2:n.-14+8186dup
ENST00000503701.1:n.352+7373dup
ENST00000504572.5:c.-14+7373dup	ENSP00000422518.1:n.-14+7373dup
ENST00000505058.5:n.241+8186dup
NM_001018074.1:c.-14+8858dup	NP_001018084.1:n.-14+8858dup
NM_001018075.1:c.-14+8955dup	NP_001018085.1:n.-14+8955dup
NM_001018077.1:c.-14+8186dup	NP_001018087.1:n.-14+8186dup
XM_005268422.2:c.-14+8186dup	XP_005268479.1:n.-14+8186dup
XM_005268422.3:c.-14+8186dup	XP_005268479.1:n.-14+8186dup
NM_001364183.1:c.-14+7373dup	NP_001351112.1:n.-14+7373dup
NM_001364183.2:c.-14+7373dup	NP_001351112.1:n.-14+7373dup