Canonical Allele Identifier: CA10585982
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 252501
ClinVar RCV Id: RCV000239160
dbSNP Id: rs879255348
MyVariant Identifiers: chr4:g.149356604G>T (hg19) chr4:g.148435452G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148435452G>T , CM000666.2:g.148435452G>T GRCh38
NC_000004.11:g.149356604G>T , CM000666.1:g.149356604G>T GRCh37
NC_000004.10:g.149576054G>T NCBI36
NG_013350.1:g.12069C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.1409C>A MANE Select ENSP00000350815.3:p.Ser470Ter
ENST00000342437.8:c.1409C>A ENSP00000343907.4:p.Ser470Ter
ENST00000344721.8:c.1409C>A ENSP00000341390.4:p.Ser470Ter
ENST00000358102.7:c.1409C>A ENSP00000350815.3:p.Ser470Ter
ENST00000511528.1:c.1409C>A ENSP00000421481.1:p.Ser470Ter
ENST00000512865.5:c.1409C>A ENSP00000423510.1:p.Ser470Ter
ENST00000625323.2:c.1409C>A ENSP00000486719.1:p.Ser470Ter
NM_000901.4:c.1409C>A NP_000892.2:p.Ser470Ter
NM_001166104.1:c.1409C>A NP_001159576.1:p.Ser470Ter
XM_011531975.1:c.1409C>A XP_011530277.1:p.Ser470Ter
XM_011531976.1:c.1409C>A XP_011530278.1:p.Ser470Ter
XM_011531977.1:c.1409C>A XP_011530279.1:p.Ser470Ter
XM_011531978.1:c.1409C>A XP_011530280.1:p.Ser470Ter
NM_001354819.1:c.1409C>A NP_001341748.1:p.Ser470Ter
NR_148974.1:n.1772C>A
XM_011531978.2:c.1409C>A XP_011530280.1:p.Ser470Ter
NM_000901.5:c.1409C>A MANE Select NP_000892.2:p.Ser470Ter
NM_001166104.2:c.1409C>A NP_001159576.1:p.Ser470Ter
NR_148974.2:n.1666C>A
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