Canonical Allele Identifier: CA2497121627

Gene: NR3C1

Linked Data

• dbSNP Id: rs1751530520

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426397del , CM000667.2:g.143426397del	GRCh38
NC_000005.9:g.142805962del , CM000667.1:g.142805962del	GRCh37
NC_000005.8:g.142786155del	NCBI36
NG_009062.1:g.14116del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8135del	ENSP00000343205.2:n.-14+8135del
ENST00000503701.1:n.352+7322del
ENST00000504572.5:c.-14+7322del	ENSP00000422518.1:n.-14+7322del
ENST00000505058.5:n.241+8135del
NM_001018074.1:c.-14+8807del	NP_001018084.1:n.-14+8807del
NM_001018075.1:c.-14+8904del	NP_001018085.1:n.-14+8904del
NM_001018077.1:c.-14+8135del	NP_001018087.1:n.-14+8135del
XM_005268422.2:c.-14+8135del	XP_005268479.1:n.-14+8135del
XM_005268422.3:c.-14+8135del	XP_005268479.1:n.-14+8135del
NM_001364183.1:c.-14+7322del	NP_001351112.1:n.-14+7322del
NM_001364183.2:c.-14+7322del	NP_001351112.1:n.-14+7322del