Canonical Allele Identifier: CA358425717

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149002617T>A (hg19) ; chr4:g.148081466T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081466T>A , CM000666.2:g.148081466T>A	GRCh38
NC_000004.11:g.149002617T>A , CM000666.1:g.149002617T>A	GRCh37
NC_000004.10:g.149222067T>A	NCBI36
NG_013350.1:g.366056A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2833A>T MANE Select	ENSP00000350815.3:p.Thr945Ser
ENST00000342437.8:c.*216A>T	ENSP00000343907.4:n.*216A>T
ENST00000344721.8:c.2833A>T	ENSP00000341390.4:p.Thr945Ser
ENST00000358102.7:c.2833A>T	ENSP00000350815.3:p.Thr945Ser
ENST00000511528.1:c.2845A>T	ENSP00000421481.1:p.Thr949Ser
ENST00000512865.5:c.2482A>T	ENSP00000423510.1:p.Thr828Ser
ENST00000625323.2:c.2845A>T	ENSP00000486719.1:p.Thr949Ser
NM_000901.4:c.2833A>T	NP_000892.2:p.Thr945Ser
NM_001166104.1:c.2482A>T	NP_001159576.1:p.Thr828Ser
XM_011531975.1:c.2845A>T	XP_011530277.1:p.Thr949Ser
XM_011531976.1:c.2845A>T	XP_011530278.1:p.Thr949Ser
XM_011531977.1:c.2845A>T	XP_011530279.1:p.Thr949Ser
NM_001354819.1:c.2482A>T	NP_001341748.1:p.Thr828Ser
NR_148974.1:n.2700A>T
NM_000901.5:c.2833A>T MANE Select	NP_000892.2:p.Thr945Ser
NM_001166104.2:c.2482A>T	NP_001159576.1:p.Thr828Ser
NR_148974.2:n.2594A>T