Canonical Allele Identifier: CA10618043
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 347691
ClinVar RCV Id: RCV000404681
dbSNP Id: rs886059122

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148079851G>A , CM000666.2:g.148079851G>A GRCh38
NC_000004.11:g.149001002G>A , CM000666.1:g.149001002G>A GRCh37
NC_000004.10:g.149220452G>A NCBI36
NG_013350.1:g.367671C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.*1493C>T MANE Select ENSP00000350815.3:n.*1493C>T
ENST00000344721.8:c.*1493C>T ENSP00000341390.4:n.*1493C>T
ENST00000358102.7:c.*1493C>T ENSP00000350815.3:n.*1493C>T
ENST00000625323.2:c.*1493C>T ENSP00000486719.1:n.*1493C>T
NM_000901.4:c.*1493C>T NP_000892.2:n.*1493C>T
NM_001166104.1:c.*1493C>T NP_001159576.1:n.*1493C>T
XM_011531975.1:c.*1493C>T XP_011530277.1:n.*1493C>T
XM_011531976.1:c.*1493C>T XP_011530278.1:n.*1493C>T
XM_011531977.1:c.*1493C>T XP_011530279.1:n.*1493C>T
NM_001354819.1:c.*1493C>T NP_001341748.1:n.*1493C>T
NR_148974.1:n.4315C>T
NM_000901.5:c.*1493C>T MANE Select NP_000892.2:n.*1493C>T
NM_001166104.2:c.*1493C>T NP_001159576.1:n.*1493C>T
NR_148974.2:n.4209C>T