Canonical Allele Identifier: CA129267712
Gene: NR3C1 HGNC NCBI

Linked Data

dbSNP Id: rs777576383

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.143426252G>T , CM000667.2:g.143426252G>T GRCh38
NC_000005.9:g.142805817G>T , CM000667.1:g.142805817G>T GRCh37
NC_000005.8:g.142786010G>T NCBI36
NG_009062.1:g.14261C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343796.6:c.-14+8280C>A ENSP00000343205.2:n.-14+8280C>A
ENST00000503701.1:n.352+7467C>A
ENST00000504572.5:c.-14+7467C>A ENSP00000422518.1:n.-14+7467C>A
ENST00000505058.5:n.241+8280C>A
NM_001018074.1:c.-14+8952C>A NP_001018084.1:n.-14+8952C>A
NM_001018075.1:c.-14+9049C>A NP_001018085.1:n.-14+9049C>A
NM_001018077.1:c.-14+8280C>A NP_001018087.1:n.-14+8280C>A
XM_005268422.2:c.-14+8280C>A XP_005268479.1:n.-14+8280C>A
XM_005268422.3:c.-14+8280C>A XP_005268479.1:n.-14+8280C>A
NM_001364183.1:c.-14+7467C>A NP_001351112.1:n.-14+7467C>A
NM_001364183.2:c.-14+7467C>A NP_001351112.1:n.-14+7467C>A