Canonical Allele Identifier: CA442002382

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149075763C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154612C>G , CM000666.2:g.148154612C>G	GRCh38
NC_000004.11:g.149075763C>G , CM000666.1:g.149075763C>G	GRCh37
NC_000004.10:g.149295213C>G	NCBI36
NG_013350.1:g.292910G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2304G>C MANE Select	ENSP00000350815.3:p.Thr768=
ENST00000342437.8:c.2015-34324G>C	ENSP00000343907.4:n.2015-34324G>C
ENST00000344721.8:c.2304G>C	ENSP00000341390.4:p.Thr768=
ENST00000358102.7:c.2304G>C	ENSP00000350815.3:p.Thr768=
ENST00000503174.1:n.233G>C
ENST00000503313.1:n.501G>C
ENST00000511528.1:c.2316G>C	ENSP00000421481.1:p.Thr772=
ENST00000512865.5:c.2015-1999G>C	ENSP00000423510.1:n.2015-1999G>C
ENST00000625323.2:c.2316G>C	ENSP00000486719.1:p.Thr772=
NM_000901.4:c.2304G>C	NP_000892.2:p.Thr768=
NM_001166104.1:c.2015-1999G>C	NP_001159576.1:n.2015-1999G>C
XM_011531975.1:c.2316G>C	XP_011530277.1:p.Thr772=
XM_011531976.1:c.2316G>C	XP_011530278.1:p.Thr772=
XM_011531977.1:c.2316G>C	XP_011530279.1:p.Thr772=
XM_011531978.1:c.2316G>C	XP_011530280.1:p.Thr772=
NM_001354819.1:c.2015-1999G>C	NP_001341748.1:n.2015-1999G>C
NR_148974.1:n.2378-34324G>C
XM_011531978.2:c.2316G>C	XP_011530280.1:p.Thr772=
NM_000901.5:c.2304G>C MANE Select	NP_000892.2:p.Thr768=
NM_001166104.2:c.2015-1999G>C	NP_001159576.1:n.2015-1999G>C
NR_148974.2:n.2272-34324G>C