Canonical Allele Identifier: CA804979225

Gene: NR3C1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143416967A>T , CM000667.2:g.143416967A>T	GRCh38
NC_000005.9:g.142796532A>T , CM000667.1:g.142796532A>T	GRCh37
NC_000005.8:g.142776725A>T	NCBI36
NG_009062.1:g.23546T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001018074.1:c.-13-16115T>A	NP_001018084.1:n.-13-16115T>A
NM_001018075.1:c.-13-16115T>A	NP_001018085.1:n.-13-16115T>A
NM_001018077.1:c.-13-16115T>A	NP_001018087.1:n.-13-16115T>A
NM_001364183.1:c.-13-16115T>A	NP_001351112.1:n.-13-16115T>A
NM_001364183.2:c.-13-16115T>A	NP_001351112.1:n.-13-16115T>A
ENST00000343796.6:c.-13-16115T>A	ENSP00000343205.2:n.-13-16115T>A
ENST00000503701.1:n.353-7728T>A
ENST00000504572.5:c.-13-16115T>A	ENSP00000422518.1:n.-13-16115T>A
ENST00000505058.5:n.242-7728T>A
XM_005268422.2:c.-13-16115T>A	XP_005268479.1:n.-13-16115T>A
XM_005268422.3:c.-13-16115T>A	XP_005268479.1:n.-13-16115T>A