Canonical Allele Identifier: CA126225
Gene: NR3C1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16151
ClinVar RCV Id: RCV000017533
dbSNP Id: rs104893909

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.143300556A>T , CM000667.2:g.143300556A>T GRCh38
NC_000005.8:g.142660314A>T NCBI36
NC_000005.9:g.142680121A>T , CM000667.1:g.142680121A>T GRCh37
NG_009062.1:g.139957T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000231509.7:c.1679T>A ENSP00000231509.3:p.Ile560Asn
ENST00000343796.6:c.1676T>A ENSP00000343205.2:p.Ile559Asn
ENST00000394464.6:c.1676T>A ENSP00000377977.2:p.Ile559Asn
ENST00000394466.6:c.1679T>A ENSP00000377979.2:p.Ile560Asn
ENST00000415690.6:c.1676T>A ENSP00000387672.2:p.Ile559Asn
ENST00000424646.6:c.1598T>A ENSP00000405282.2:p.Ile533Asn
ENST00000503201.1:c.1676T>A ENSP00000427672.1:p.Ile559Asn
ENST00000504572.5:c.1679T>A ENSP00000422518.1:p.Ile560Asn
NM_000176.2:c.1676T>A VV NP_000167.1:p.Ile559Asn
NM_001018074.1:c.1676T>A VV NP_001018084.1:p.Ile559Asn
NM_001018075.1:c.1676T>A VV NP_001018085.1:p.Ile559Asn
NM_001018076.1:c.1676T>A VV NP_001018086.1:p.Ile559Asn
NM_001018077.1:c.1676T>A VV NP_001018087.1:p.Ile559Asn
NM_001020825.1:c.1676T>A VV NP_001018661.1:p.Ile559Asn
NM_001024094.1:c.1679T>A VV NP_001019265.1:p.Ile560Asn
NM_001204258.1:c.1598T>A VV NP_001191187.1:p.Ile533Asn
NM_001204259.1:c.1421T>A VV NP_001191188.1:p.Ile474Asn
NM_001204260.1:c.1409T>A VV NP_001191189.1:p.Ile470Asn
NM_001204261.1:c.1385T>A VV NP_001191190.1:p.Ile462Asn
NM_001204262.1:c.731T>A VV NP_001191191.1:p.Ile244Asn
NM_001204263.1:c.686T>A VV NP_001191192.1:p.Ile229Asn
NM_001204264.1:c.671T>A VV NP_001191193.1:p.Ile224Asn
NM_001204265.1:c.1676T>A VV NP_001191194.1:p.Ile559Asn
XM_005268419.2:c.1679T>A XP_005268476.1:p.Ile560Asn
XM_005268420.3:c.1679T>A XP_005268477.1:p.Ile560Asn
XM_005268422.2:c.1679T>A XP_005268479.1:p.Ile560Asn
XM_005268423.2:c.1679T>A XP_005268480.1:p.Ile560Asn
XM_011537637.1:c.485T>A XP_011535939.1:p.Ile162Asn