Canonical Allele Identifier: CA10620197

Gene: NR3C2

Linked Data

• ClinVar Variation Id: 347683
• ClinVar RCV Id: RCV000264896
• dbSNP Id: rs5536
• gnomAD v2: 4-149000693-C-T
• gnomAD v3: 4-148079542-C-T
• gnomAD v4: 4-148079542-C-T
• MyVariant Identifiers: chr4:g.149000693C>T (hg19) ; chr4:g.148079542C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148079542C>T , CM000666.2:g.148079542C>T	GRCh38
NC_000004.11:g.149000693C>T , CM000666.1:g.149000693C>T	GRCh37
NC_000004.10:g.149220143C>T	NCBI36
NG_013350.1:g.367980G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.*1802G>A MANE Select	ENSP00000350815.3:n.*1802G>A
ENST00000344721.8:c.*1802G>A	ENSP00000341390.4:n.*1802G>A
ENST00000358102.7:c.*1802G>A	ENSP00000350815.3:n.*1802G>A
ENST00000625323.2:c.*1802G>A	ENSP00000486719.1:n.*1802G>A
NM_000901.4:c.*1802G>A	NP_000892.2:n.*1802G>A
NM_001166104.1:c.*1802G>A	NP_001159576.1:n.*1802G>A
XM_011531975.1:c.*1802G>A	XP_011530277.1:n.*1802G>A
XM_011531976.1:c.*1802G>A	XP_011530278.1:n.*1802G>A
XM_011531977.1:c.*1802G>A	XP_011530279.1:n.*1802G>A
NM_001354819.1:c.*1802G>A	NP_001341748.1:n.*1802G>A
NR_148974.1:n.4624G>A
NM_000901.5:c.*1802G>A MANE Select	NP_000892.2:n.*1802G>A
NM_001166104.2:c.*1802G>A	NP_001159576.1:n.*1802G>A
NR_148974.2:n.4518G>A