Canonical Allele Identifier: CA108485440
Gene: NR3C2 HGNC NCBI

Linked Data

dbSNP Id: rs942375084

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152518G>A , CM000666.2:g.148152518G>A GRCh38
NC_000004.11:g.149073669G>A , CM000666.1:g.149073669G>A GRCh37
NC_000004.10:g.149293119G>A NCBI36
NG_013350.1:g.295004C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358102.8:c.2461C>T MANE Select ENSP00000350815.3:p.His821Tyr
ENST00000342437.8:c.2015-32230C>T ENSP00000343907.4:n.2015-32230C>T
ENST00000344721.8:c.2461C>T ENSP00000341390.4:p.His821Tyr
ENST00000358102.7:c.2461C>T ENSP00000350815.3:p.His821Tyr
ENST00000503174.1:n.390C>T
ENST00000503313.1:n.658C>T
ENST00000511528.1:c.2473C>T ENSP00000421481.1:p.His825Tyr
ENST00000512865.5:c.2110C>T ENSP00000423510.1:p.His704Tyr
ENST00000625323.2:c.2473C>T ENSP00000486719.1:p.His825Tyr
NM_000901.4:c.2461C>T NP_000892.2:p.His821Tyr
NM_001166104.1:c.2110C>T NP_001159576.1:p.His704Tyr
XM_011531975.1:c.2473C>T XP_011530277.1:p.His825Tyr
XM_011531976.1:c.2473C>T XP_011530278.1:p.His825Tyr
XM_011531977.1:c.2473C>T XP_011530279.1:p.His825Tyr
XM_011531978.1:c.2473C>T XP_011530280.1:p.His825Tyr
NM_001354819.1:c.2110C>T NP_001341748.1:p.His704Tyr
NR_148974.1:n.2378-32230C>T
XM_011531978.2:c.2473C>T XP_011530280.1:p.His825Tyr
NM_000901.5:c.2461C>T MANE Select NP_000892.2:p.His821Tyr
NM_001166104.2:c.2110C>T NP_001159576.1:p.His704Tyr
NR_148974.2:n.2272-32230C>T