Canonical Allele Identifier: CA2710103357

Gene: NR3C1

Linked Data

• dbSNP Id: rs1751770688

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143430629C>T , CM000667.2:g.143430629C>T	GRCh38
NC_000005.9:g.142810194C>T , CM000667.1:g.142810194C>T	GRCh37
NC_000005.8:g.142790387C>T	NCBI36
NG_009062.1:g.9884G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+3903G>A	ENSP00000343205.2:n.-14+3903G>A
ENST00000503701.1:n.352+3090G>A
ENST00000504572.5:c.-14+3090G>A	ENSP00000422518.1:n.-14+3090G>A
ENST00000505058.5:n.241+3903G>A
NM_001018074.1:c.-14+4575G>A	NP_001018084.1:n.-14+4575G>A
NM_001018075.1:c.-14+4672G>A	NP_001018085.1:n.-14+4672G>A
NM_001018077.1:c.-14+3903G>A	NP_001018087.1:n.-14+3903G>A
XM_005268422.2:c.-14+3903G>A	XP_005268479.1:n.-14+3903G>A
XM_005268422.3:c.-14+3903G>A	XP_005268479.1:n.-14+3903G>A
NM_001364183.1:c.-14+3090G>A	NP_001351112.1:n.-14+3090G>A
NM_001364183.2:c.-14+3090G>A	NP_001351112.1:n.-14+3090G>A