Canonical Allele Identifier: CA2580591132

Gene: NR3C1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143413425T= , CM000667.2:g.143413425T=	GRCh38
NC_000005.9:g.142792990T= , CM000667.1:g.142792990T=	GRCh37
NC_000005.8:g.142773183T=	NCBI36
NG_009062.1:g.27088A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001018074.1:c.-13-12573A=	NP_001018084.1:n.-13-12573A=
NM_001018075.1:c.-13-12573A=	NP_001018085.1:n.-13-12573A=
NM_001018077.1:c.-13-12573A=	NP_001018087.1:n.-13-12573A=
NM_001364183.1:c.-13-12573A=	NP_001351112.1:n.-13-12573A=
NM_001364183.2:c.-13-12573A=	NP_001351112.1:n.-13-12573A=
ENST00000343796.6:c.-13-12573A=	ENSP00000343205.2:n.-13-12573A=
ENST00000503701.1:n.353-4186A=
ENST00000504572.5:c.-13-12573A=	ENSP00000422518.1:n.-13-12573A=
ENST00000505058.5:n.242-4186A=
XM_005268422.2:c.-13-12573A=	XP_005268479.1:n.-13-12573A=
XM_005268422.3:c.-13-12573A=	XP_005268479.1:n.-13-12573A=