Canonical Allele Identifier: CA3100094
Gene: NR3C2 HGNC NCBI

Linked Data

dbSNP Id: rs750640055

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148152450C>T , CM000666.2:g.148152450C>T GRCh38
NC_000004.11:g.149073601C>T , CM000666.1:g.149073601C>T GRCh37
NC_000004.10:g.149293051C>T NCBI36
NG_013350.1:g.295072G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.2510+19G>A MANE Select ENSP00000350815.3:n.2510+19G>A
ENST00000342437.8:c.2015-32162G>A ENSP00000343907.4:n.2015-32162G>A
ENST00000344721.8:c.2510+19G>A ENSP00000341390.4:n.2510+19G>A
ENST00000358102.7:c.2510+19G>A ENSP00000350815.3:n.2510+19G>A
ENST00000503174.1:n.458G>A
ENST00000503313.1:n.707+19G>A
ENST00000511528.1:c.2522+19G>A ENSP00000421481.1:n.2522+19G>A
ENST00000512865.5:c.2159+19G>A ENSP00000423510.1:n.2159+19G>A
ENST00000625323.2:c.2522+19G>A ENSP00000486719.1:n.2522+19G>A
NM_000901.4:c.2510+19G>A NP_000892.2:n.2510+19G>A
NM_001166104.1:c.2159+19G>A NP_001159576.1:n.2159+19G>A
XM_011531975.1:c.2522+19G>A XP_011530277.1:n.2522+19G>A
XM_011531976.1:c.2522+19G>A XP_011530278.1:n.2522+19G>A
XM_011531977.1:c.2522+19G>A XP_011530279.1:n.2522+19G>A
XM_011531978.1:c.2522+19G>A XP_011530280.1:n.2522+19G>A
NM_001354819.1:c.2159+19G>A NP_001341748.1:n.2159+19G>A
NR_148974.1:n.2378-32162G>A
XM_011531978.2:c.2522+19G>A XP_011530280.1:n.2522+19G>A
NM_000901.5:c.2510+19G>A MANE Select NP_000892.2:n.2510+19G>A
NM_001166104.2:c.2159+19G>A NP_001159576.1:n.2159+19G>A
NR_148974.2:n.2272-32162G>A