Canonical Allele Identifier: CA441755224

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149115979A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148194828A>G , CM000666.2:g.148194828A>G	GRCh38
NC_000004.11:g.149115979A>G , CM000666.1:g.149115979A>G	GRCh37
NC_000004.10:g.149335429A>G	NCBI36
NG_013350.1:g.252694T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.1932T>C MANE Select	ENSP00000350815.3:p.Asp644=
ENST00000342437.8:c.1932T>C	ENSP00000343907.4:p.Asp644=
ENST00000344721.8:c.1932T>C	ENSP00000341390.4:p.Asp644=
ENST00000358102.7:c.1932T>C	ENSP00000350815.3:p.Asp644=
ENST00000503313.1:n.129T>C
ENST00000504753.1:n.381T>C
ENST00000511528.1:c.1944T>C	ENSP00000421481.1:p.Asp648=
ENST00000512865.5:c.1932T>C	ENSP00000423510.1:p.Asp644=
ENST00000625323.2:c.1944T>C	ENSP00000486719.1:p.Asp648=
NM_000901.4:c.1932T>C	NP_000892.2:p.Asp644=
NM_001166104.1:c.1932T>C	NP_001159576.1:p.Asp644=
XM_011531975.1:c.1944T>C	XP_011530277.1:p.Asp648=
XM_011531976.1:c.1944T>C	XP_011530278.1:p.Asp648=
XM_011531977.1:c.1944T>C	XP_011530279.1:p.Asp648=
XM_011531978.1:c.1944T>C	XP_011530280.1:p.Asp648=
NM_001354819.1:c.1932T>C	NP_001341748.1:p.Asp644=
NR_148974.1:n.2295T>C
XM_011531978.2:c.1944T>C	XP_011530280.1:p.Asp648=
NM_000901.5:c.1932T>C MANE Select	NP_000892.2:p.Asp644=
NM_001166104.2:c.1932T>C	NP_001159576.1:p.Asp644=
NR_148974.2:n.2189T>C