Canonical Allele Identifier: CA442017602

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149357917T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148436765T>C , CM000666.2:g.148436765T>C	GRCh38
NC_000004.11:g.149357917T>C , CM000666.1:g.149357917T>C	GRCh37
NC_000004.10:g.149577367T>C	NCBI36
NG_013350.1:g.10756A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.96A>G MANE Select	ENSP00000350815.3:p.Gly32=
ENST00000342437.8:c.96A>G	ENSP00000343907.4:p.Gly32=
ENST00000344721.8:c.96A>G	ENSP00000341390.4:p.Gly32=
ENST00000358102.7:c.96A>G	ENSP00000350815.3:p.Gly32=
ENST00000511528.1:c.96A>G	ENSP00000421481.1:p.Gly32=
ENST00000512865.5:c.96A>G	ENSP00000423510.1:p.Gly32=
ENST00000625323.2:c.96A>G	ENSP00000486719.1:p.Gly32=
NM_000901.4:c.96A>G	NP_000892.2:p.Gly32=
NM_001166104.1:c.96A>G	NP_001159576.1:p.Gly32=
XM_011531975.1:c.96A>G	XP_011530277.1:p.Gly32=
XM_011531976.1:c.96A>G	XP_011530278.1:p.Gly32=
XM_011531977.1:c.96A>G	XP_011530279.1:p.Gly32=
XM_011531978.1:c.96A>G	XP_011530280.1:p.Gly32=
NM_001354819.1:c.96A>G	NP_001341748.1:p.Gly32=
NR_148974.1:n.459A>G
XM_011531978.2:c.96A>G	XP_011530280.1:p.Gly32=
NM_000901.5:c.96A>G MANE Select	NP_000892.2:p.Gly32=
NM_001166104.2:c.96A>G	NP_001159576.1:p.Gly32=
NR_148974.2:n.353A>G