Canonical Allele Identifier: CA358425415
Gene: NR3C2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152479C>A , CM000666.2:g.148152479C>A GRCh38
NC_000004.11:g.149073630C>A , CM000666.1:g.149073630C>A GRCh37
NC_000004.10:g.149293080C>A NCBI36
NG_013350.1:g.295043G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.2500G>T MANE Select ENSP00000350815.3:p.Val834Phe
ENST00000342437.8:c.2015-32191G>T ENSP00000343907.4:p.=
ENST00000344721.8:c.2500G>T ENSP00000341390.4:p.Val834Phe
ENST00000358102.7:c.2500G>T ENSP00000350815.3:p.Val834Phe
ENST00000503174.1:n.429G>T
ENST00000503313.1:n.697G>T
ENST00000511528.1:n.2512G>T ENSP00000421481.1:p.Val838Phe
ENST00000512865.5:c.2149G>T ENSP00000423510.1:p.Val717Phe
ENST00000625323.2:c.2512G>T ENSP00000486719.1:p.Val838Phe
NM_000901.4:c.2500G>T NP_000892.2:p.Val834Phe
NM_001166104.1:c.2149G>T NP_001159576.1:p.Val717Phe
XM_011531975.1:c.2512G>T XP_011530277.1:p.Val838Phe
XM_011531976.1:c.2512G>T XP_011530278.1:p.Val838Phe
XM_011531977.1:c.2512G>T XP_011530279.1:p.Val838Phe
XM_011531978.1:c.2512G>T XP_011530280.1:p.Val838Phe
NM_001354819.1:c.2149G>T NP_001341748.1:p.Val717Phe
NR_148974.1:n.2378-32191G>T
XM_011531978.2:c.2512G>T XP_011530280.1:p.Val838Phe
NM_000901.5:c.2500G>T MANE Select NP_000892.2:p.Val834Phe
NM_001166104.2:c.2149G>T NP_001159576.1:p.Val717Phe
NR_148974.2:n.2272-32191G>T