Canonical Allele Identifier: CA1502448379

Gene: NR3C2

Linked Data

• dbSNP Id: rs1741170966

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148280354G>C , CM000666.2:g.148280354G>C	GRCh38
NC_000004.11:g.149201506G>C , CM000666.1:g.149201506G>C	GRCh37
NC_000004.10:g.149420956G>C	NCBI36
NG_013350.1:g.167167C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.1758-20237C>G MANE Select	ENSP00000350815.3:n.1758-20237C>G
ENST00000342437.8:c.1758-20237C>G	ENSP00000343907.4:n.1758-20237C>G
ENST00000344721.8:c.1758-20237C>G	ENSP00000341390.4:n.1758-20237C>G
ENST00000358102.7:c.1758-20237C>G	ENSP00000350815.3:n.1758-20237C>G
ENST00000504753.1:n.207-20237C>G
ENST00000511528.1:c.1758-20237C>G	ENSP00000421481.1:n.1758-20237C>G
ENST00000512865.5:c.1758-20237C>G	ENSP00000423510.1:n.1758-20237C>G
ENST00000625323.2:c.1758-20237C>G	ENSP00000486719.1:n.1758-20237C>G
NM_000901.4:c.1758-20237C>G	NP_000892.2:n.1758-20237C>G
NM_001166104.1:c.1758-20237C>G	NP_001159576.1:n.1758-20237C>G
XM_011531975.1:c.1758-20237C>G	XP_011530277.1:n.1758-20237C>G
XM_011531976.1:c.1758-20237C>G	XP_011530278.1:n.1758-20237C>G
XM_011531977.1:c.1758-20237C>G	XP_011530279.1:n.1758-20237C>G
XM_011531978.1:c.1758-20237C>G	XP_011530280.1:n.1758-20237C>G
NM_001354819.1:c.1758-20237C>G	NP_001341748.1:n.1758-20237C>G
NR_148974.1:n.2121-20237C>G
XM_011531978.2:c.1758-20237C>G	XP_011530280.1:n.1758-20237C>G
NM_000901.5:c.1758-20237C>G MANE Select	NP_000892.2:n.1758-20237C>G
NM_001166104.2:c.1758-20237C>G	NP_001159576.1:n.1758-20237C>G
NR_148974.2:n.2015-20237C>G