Canonical Allele Identifier: CA2675771267

Gene: NR3C1

Linked Data

• dbSNP Id: rs1001466183
• gnomAD v4: 5-143407387-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143407394_143407395dup , CM000667.2:g.143407394_143407395dup	GRCh38
NC_000005.9:g.142786959_142786960dup , CM000667.1:g.142786959_142786960dup	GRCh37
NC_000005.8:g.142767152_142767153dup	NCBI36
NG_009062.1:g.33124_33125dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-13-6537_-13-6536dup	ENSP00000343205.2:n.-13-6537_-13-6536dup
ENST00000504572.5:c.-13-6537_-13-6536dup	ENSP00000422518.1:n.-13-6537_-13-6536dup
NM_001018074.1:c.-13-6537_-13-6536dup	NP_001018084.1:n.-13-6537_-13-6536dup
NM_001018075.1:c.-13-6537_-13-6536dup	NP_001018085.1:n.-13-6537_-13-6536dup
NM_001018077.1:c.-13-6537_-13-6536dup	NP_001018087.1:n.-13-6537_-13-6536dup
XM_005268422.2:c.-13-6537_-13-6536dup	XP_005268479.1:n.-13-6537_-13-6536dup
XM_005268422.3:c.-13-6537_-13-6536dup	XP_005268479.1:n.-13-6537_-13-6536dup
NM_001364183.1:c.-13-6537_-13-6536dup	NP_001351112.1:n.-13-6537_-13-6536dup
NM_001364183.2:c.-13-6537_-13-6536dup	NP_001351112.1:n.-13-6537_-13-6536dup