Canonical Allele Identifier: CA10618046

Gene: NR3C2

Linked Data

• ClinVar Variation Id: 347692
• ClinVar RCV Id: RCV000294136
• dbSNP Id: rs886059123
• gnomAD v2: 4-149001020-A-C
• gnomAD v3: 4-148079869-A-C
• gnomAD v4: 4-148079869-A-C
• MyVariant Identifiers: chr4:g.149001020A>C (hg19) ; chr4:g.148079869A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148079869A>C , CM000666.2:g.148079869A>C	GRCh38
NC_000004.11:g.149001020A>C , CM000666.1:g.149001020A>C	GRCh37
NC_000004.10:g.149220470A>C	NCBI36
NG_013350.1:g.367653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.*1475T>G MANE Select	ENSP00000350815.3:n.*1475T>G
ENST00000344721.8:c.*1475T>G	ENSP00000341390.4:n.*1475T>G
ENST00000358102.7:c.*1475T>G	ENSP00000350815.3:n.*1475T>G
ENST00000625323.2:c.*1475T>G	ENSP00000486719.1:n.*1475T>G
NM_000901.4:c.*1475T>G	NP_000892.2:n.*1475T>G
NM_001166104.1:c.*1475T>G	NP_001159576.1:n.*1475T>G
XM_011531975.1:c.*1475T>G	XP_011530277.1:n.*1475T>G
XM_011531976.1:c.*1475T>G	XP_011530278.1:n.*1475T>G
XM_011531977.1:c.*1475T>G	XP_011530279.1:n.*1475T>G
NM_001354819.1:c.*1475T>G	NP_001341748.1:n.*1475T>G
NR_148974.1:n.4297T>G
NM_000901.5:c.*1475T>G MANE Select	NP_000892.2:n.*1475T>G
NM_001166104.2:c.*1475T>G	NP_001159576.1:n.*1475T>G
NR_148974.2:n.4191T>G