Canonical Allele Identifier: CA129265770
Gene: NR3C1 HGNC NCBI

Linked Data

dbSNP Id: rs778193638

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.143407048A>G , CM000667.2:g.143407048A>G GRCh38
NC_000005.9:g.142786613A>G , CM000667.1:g.142786613A>G GRCh37
NC_000005.8:g.142766806A>G NCBI36
NG_009062.1:g.33465T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343796.6:c.-13-6196T>C ENSP00000343205.2:n.-13-6196T>C
ENST00000504572.5:c.-13-6196T>C ENSP00000422518.1:n.-13-6196T>C
NM_001018074.1:c.-13-6196T>C NP_001018084.1:n.-13-6196T>C
NM_001018075.1:c.-13-6196T>C NP_001018085.1:n.-13-6196T>C
NM_001018077.1:c.-13-6196T>C NP_001018087.1:n.-13-6196T>C
XM_005268422.2:c.-13-6196T>C XP_005268479.1:n.-13-6196T>C
XM_005268422.3:c.-13-6196T>C XP_005268479.1:n.-13-6196T>C
NM_001364183.1:c.-13-6196T>C NP_001351112.1:n.-13-6196T>C
NM_001364183.2:c.-13-6196T>C NP_001351112.1:n.-13-6196T>C