Canonical Allele Identifier: CA129267720

Gene: NR3C1

Linked Data

• dbSNP Id: rs989490078
• MyVariant Identifiers: chr5:g.142805908G>A (hg19) ; chr5:g.143426343G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426343G>A , CM000667.2:g.143426343G>A	GRCh38
NC_000005.9:g.142805908G>A , CM000667.1:g.142805908G>A	GRCh37
NC_000005.8:g.142786101G>A	NCBI36
NG_009062.1:g.14170C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8189C>T	ENSP00000343205.2:n.-14+8189C>T
ENST00000503701.1:n.352+7376C>T
ENST00000504572.5:c.-14+7376C>T	ENSP00000422518.1:n.-14+7376C>T
ENST00000505058.5:n.241+8189C>T
NM_001018074.1:c.-14+8861C>T	NP_001018084.1:n.-14+8861C>T
NM_001018075.1:c.-14+8958C>T	NP_001018085.1:n.-14+8958C>T
NM_001018077.1:c.-14+8189C>T	NP_001018087.1:n.-14+8189C>T
XM_005268422.2:c.-14+8189C>T	XP_005268479.1:n.-14+8189C>T
XM_005268422.3:c.-14+8189C>T	XP_005268479.1:n.-14+8189C>T
NM_001364183.1:c.-14+7376C>T	NP_001351112.1:n.-14+7376C>T
NM_001364183.2:c.-14+7376C>T	NP_001351112.1:n.-14+7376C>T