Canonical Allele Identifier: CA441755226

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149115982A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148194831A>G , CM000666.2:g.148194831A>G	GRCh38
NC_000004.11:g.149115982A>G , CM000666.1:g.149115982A>G	GRCh37
NC_000004.10:g.149335432A>G	NCBI36
NG_013350.1:g.252691T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.1929T>C MANE Select	ENSP00000350815.3:p.Asn643=
ENST00000342437.8:c.1929T>C	ENSP00000343907.4:p.Asn643=
ENST00000344721.8:c.1929T>C	ENSP00000341390.4:p.Asn643=
ENST00000358102.7:c.1929T>C	ENSP00000350815.3:p.Asn643=
ENST00000503313.1:n.126T>C
ENST00000504753.1:n.378T>C
ENST00000511528.1:c.1941T>C	ENSP00000421481.1:p.Asn647=
ENST00000512865.5:c.1929T>C	ENSP00000423510.1:p.Asn643=
ENST00000625323.2:c.1941T>C	ENSP00000486719.1:p.Asn647=
NM_000901.4:c.1929T>C	NP_000892.2:p.Asn643=
NM_001166104.1:c.1929T>C	NP_001159576.1:p.Asn643=
XM_011531975.1:c.1941T>C	XP_011530277.1:p.Asn647=
XM_011531976.1:c.1941T>C	XP_011530278.1:p.Asn647=
XM_011531977.1:c.1941T>C	XP_011530279.1:p.Asn647=
XM_011531978.1:c.1941T>C	XP_011530280.1:p.Asn647=
NM_001354819.1:c.1929T>C	NP_001341748.1:p.Asn643=
NR_148974.1:n.2292T>C
XM_011531978.2:c.1941T>C	XP_011530280.1:p.Asn647=
NM_000901.5:c.1929T>C MANE Select	NP_000892.2:p.Asn643=
NM_001166104.2:c.1929T>C	NP_001159576.1:p.Asn643=
NR_148974.2:n.2186T>C