Canonical Allele Identifier: CA1082404604
Gene: NR3C1 HGNC NCBI

Linked Data

dbSNP Id: rs1841141484

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.143407173A>T , CM000667.2:g.143407173A>T GRCh38
NC_000005.9:g.142786738A>T , CM000667.1:g.142786738A>T GRCh37
NC_000005.8:g.142766931A>T NCBI36
NG_009062.1:g.33340T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343796.6:c.-13-6321T>A ENSP00000343205.2:n.-13-6321T>A
ENST00000504572.5:c.-13-6321T>A ENSP00000422518.1:n.-13-6321T>A
NM_001018074.1:c.-13-6321T>A NP_001018084.1:n.-13-6321T>A
NM_001018075.1:c.-13-6321T>A NP_001018085.1:n.-13-6321T>A
NM_001018077.1:c.-13-6321T>A NP_001018087.1:n.-13-6321T>A
XM_005268422.2:c.-13-6321T>A XP_005268479.1:n.-13-6321T>A
XM_005268422.3:c.-13-6321T>A XP_005268479.1:n.-13-6321T>A
NM_001364183.1:c.-13-6321T>A NP_001351112.1:n.-13-6321T>A
NM_001364183.2:c.-13-6321T>A NP_001351112.1:n.-13-6321T>A