Canonical Allele Identifier: CA804983241

Gene: NR3C1

Linked Data

• dbSNP Id: rs1317703103
• gnomAD v3: 5-143426246-C-T
• gnomAD v4: 5-143426246-C-T
• MyVariant Identifiers: chr5:g.142805811C>T (hg19) ; chr5:g.143426246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426246C>T , CM000667.2:g.143426246C>T	GRCh38
NC_000005.9:g.142805811C>T , CM000667.1:g.142805811C>T	GRCh37
NC_000005.8:g.142786004C>T	NCBI36
NG_009062.1:g.14267G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8286G>A	ENSP00000343205.2:n.-14+8286G>A
ENST00000503701.1:n.352+7473G>A
ENST00000504572.5:c.-14+7473G>A	ENSP00000422518.1:n.-14+7473G>A
ENST00000505058.5:n.241+8286G>A
NM_001018074.1:c.-14+8958G>A	NP_001018084.1:n.-14+8958G>A
NM_001018075.1:c.-14+9055G>A	NP_001018085.1:n.-14+9055G>A
NM_001018077.1:c.-14+8286G>A	NP_001018087.1:n.-14+8286G>A
XM_005268422.2:c.-14+8286G>A	XP_005268479.1:n.-14+8286G>A
XM_005268422.3:c.-14+8286G>A	XP_005268479.1:n.-14+8286G>A
NM_001364183.1:c.-14+7473G>A	NP_001351112.1:n.-14+7473G>A
NM_001364183.2:c.-14+7473G>A	NP_001351112.1:n.-14+7473G>A