Canonical Allele Identifier: CA2581501789

Gene: NR3C1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143427467G= , CM000667.2:g.143427467G=	GRCh38
NC_000005.9:g.142807032G= , CM000667.1:g.142807032G=	GRCh37
NC_000005.8:g.142787225G=	NCBI36
NG_009062.1:g.13046C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001018074.1:c.-14+7737C=	NP_001018084.1:n.-14+7737C=
NM_001018075.1:c.-14+7834C=	NP_001018085.1:n.-14+7834C=
NM_001018077.1:c.-14+7065C=	NP_001018087.1:n.-14+7065C=
NM_001364183.1:c.-14+6252C=	NP_001351112.1:n.-14+6252C=
NM_001364183.2:c.-14+6252C=	NP_001351112.1:n.-14+6252C=
ENST00000343796.6:c.-14+7065C=	ENSP00000343205.2:n.-14+7065C=
ENST00000503701.1:n.352+6252C=
ENST00000504572.5:c.-14+6252C=	ENSP00000422518.1:n.-14+6252C=
ENST00000505058.5:n.241+7065C=
XM_005268422.2:c.-14+7065C=	XP_005268479.1:n.-14+7065C=
XM_005268422.3:c.-14+7065C=	XP_005268479.1:n.-14+7065C=