Canonical Allele Identifier: CA2497121450

Gene: NR3C1

Linked Data

• dbSNP Id: rs1841134862

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143406959_143406962del , CM000667.2:g.143406959_143406962del	GRCh38
NC_000005.9:g.142786524_142786527del , CM000667.1:g.142786524_142786527del	GRCh37
NC_000005.8:g.142766717_142766720del	NCBI36
NG_009062.1:g.33551_33554del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-13-6110_-13-6107del	ENSP00000343205.2:n.-13-6110_-13-6107del
ENST00000504572.5:c.-13-6110_-13-6107del	ENSP00000422518.1:n.-13-6110_-13-6107del
NM_001018074.1:c.-13-6110_-13-6107del	NP_001018084.1:n.-13-6110_-13-6107del
NM_001018075.1:c.-13-6110_-13-6107del	NP_001018085.1:n.-13-6110_-13-6107del
NM_001018077.1:c.-13-6110_-13-6107del	NP_001018087.1:n.-13-6110_-13-6107del
XM_005268422.2:c.-13-6110_-13-6107del	XP_005268479.1:n.-13-6110_-13-6107del
XM_005268422.3:c.-13-6110_-13-6107del	XP_005268479.1:n.-13-6110_-13-6107del
NM_001364183.1:c.-13-6110_-13-6107del	NP_001351112.1:n.-13-6110_-13-6107del
NM_001364183.2:c.-13-6110_-13-6107del	NP_001351112.1:n.-13-6110_-13-6107del