Canonical Allele Identifier: CA1502331263
Gene: NR3C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148081279G= , CM000666.2:g.148081279G= GRCh38
NC_000004.11:g.149002430G= , CM000666.1:g.149002430G= GRCh37
NC_000004.10:g.149221880G= NCBI36
NG_013350.1:g.366243C=

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.*65C= MANE Select ENSP00000350815.3:n.*65C=
ENST00000342437.8:c.*403C= ENSP00000343907.4:n.*403C=
ENST00000344721.8:c.*65C= ENSP00000341390.4:n.*65C=
ENST00000358102.7:c.*65C= ENSP00000350815.3:n.*65C=
ENST00000512865.5:c.*65C= ENSP00000423510.1:n.*65C=
ENST00000625323.2:c.*65C= ENSP00000486719.1:n.*65C=
NM_000901.4:c.*65C= NP_000892.2:n.*65C=
NM_001166104.1:c.*65C= NP_001159576.1:n.*65C=
XM_011531975.1:c.*65C= XP_011530277.1:n.*65C=
XM_011531976.1:c.*65C= XP_011530278.1:n.*65C=
XM_011531977.1:c.*65C= XP_011530279.1:n.*65C=
NM_001354819.1:c.*65C= NP_001341748.1:n.*65C=
NR_148974.1:n.2887C=
NM_000901.5:c.*65C= MANE Select NP_000892.2:n.*65C=
NM_001166104.2:c.*65C= NP_001159576.1:n.*65C=
NR_148974.2:n.2781C=