Canonical Allele Identifier: CA358426716

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149075953T>A (hg19) ; chr4:g.148154802T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154802T>A , CM000666.2:g.148154802T>A	GRCh38
NC_000004.11:g.149075953T>A , CM000666.1:g.149075953T>A	GRCh37
NC_000004.10:g.149295403T>A	NCBI36
NG_013350.1:g.292720A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2114A>T MANE Select	ENSP00000350815.3:p.Glu705Val
ENST00000342437.8:c.2015-34514A>T	ENSP00000343907.4:n.2015-34514A>T
ENST00000344721.8:c.2114A>T	ENSP00000341390.4:p.Glu705Val
ENST00000358102.7:c.2114A>T	ENSP00000350815.3:p.Glu705Val
ENST00000503174.1:n.43A>T
ENST00000503313.1:n.311A>T
ENST00000511528.1:c.2126A>T	ENSP00000421481.1:p.Glu709Val
ENST00000512865.5:c.2015-2189A>T	ENSP00000423510.1:n.2015-2189A>T
ENST00000625323.2:c.2126A>T	ENSP00000486719.1:p.Glu709Val
NM_000901.4:c.2114A>T	NP_000892.2:p.Glu705Val
NM_001166104.1:c.2015-2189A>T	NP_001159576.1:n.2015-2189A>T
XM_011531975.1:c.2126A>T	XP_011530277.1:p.Glu709Val
XM_011531976.1:c.2126A>T	XP_011530278.1:p.Glu709Val
XM_011531977.1:c.2126A>T	XP_011530279.1:p.Glu709Val
XM_011531978.1:c.2126A>T	XP_011530280.1:p.Glu709Val
NM_001354819.1:c.2015-2189A>T	NP_001341748.1:n.2015-2189A>T
NR_148974.1:n.2378-34514A>T
XM_011531978.2:c.2126A>T	XP_011530280.1:p.Glu709Val
NM_000901.5:c.2114A>T MANE Select	NP_000892.2:p.Glu705Val
NM_001166104.2:c.2015-2189A>T	NP_001159576.1:n.2015-2189A>T
NR_148974.2:n.2272-34514A>T