Canonical Allele Identifier: CA10617176

Gene: NR3C2

Linked Data

• ClinVar Variation Id: 347696
• ClinVar RCV Id: RCV000360227
• dbSNP Id: rs61763137
• gnomAD v2: 4-149001089-T-A
• gnomAD v3: 4-148079938-T-A
• gnomAD v4: 4-148079938-T-A
• MyVariant Identifiers: chr4:g.149001089T>A (hg19) ; chr4:g.148079938T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148079938T>A , CM000666.2:g.148079938T>A	GRCh38
NC_000004.11:g.149001089T>A , CM000666.1:g.149001089T>A	GRCh37
NC_000004.10:g.149220539T>A	NCBI36
NG_013350.1:g.367584A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.*1406A>T MANE Select	ENSP00000350815.3:n.*1406A>T
ENST00000344721.8:c.*1406A>T	ENSP00000341390.4:n.*1406A>T
ENST00000358102.7:c.*1406A>T	ENSP00000350815.3:n.*1406A>T
ENST00000625323.2:c.*1406A>T	ENSP00000486719.1:n.*1406A>T
NM_000901.4:c.*1406A>T	NP_000892.2:n.*1406A>T
NM_001166104.1:c.*1406A>T	NP_001159576.1:n.*1406A>T
XM_011531975.1:c.*1406A>T	XP_011530277.1:n.*1406A>T
XM_011531976.1:c.*1406A>T	XP_011530278.1:n.*1406A>T
XM_011531977.1:c.*1406A>T	XP_011530279.1:n.*1406A>T
NM_001354819.1:c.*1406A>T	NP_001341748.1:n.*1406A>T
NR_148974.1:n.4228A>T
NM_000901.5:c.*1406A>T MANE Select	NP_000892.2:n.*1406A>T
NM_001166104.2:c.*1406A>T	NP_001159576.1:n.*1406A>T
NR_148974.2:n.4122A>T