Canonical Allele Identifier: CA358425708

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149002616G>C (hg19) ; chr4:g.148081465G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081465G>C , CM000666.2:g.148081465G>C	GRCh38
NC_000004.11:g.149002616G>C , CM000666.1:g.149002616G>C	GRCh37
NC_000004.10:g.149222066G>C	NCBI36
NG_013350.1:g.366057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2834C>G MANE Select	ENSP00000350815.3:p.Thr945Ser
ENST00000342437.8:c.*217C>G	ENSP00000343907.4:n.*217C>G
ENST00000344721.8:c.2834C>G	ENSP00000341390.4:p.Thr945Ser
ENST00000358102.7:c.2834C>G	ENSP00000350815.3:p.Thr945Ser
ENST00000511528.1:c.2846C>G	ENSP00000421481.1:p.Thr949Ser
ENST00000512865.5:c.2483C>G	ENSP00000423510.1:p.Thr828Ser
ENST00000625323.2:c.2846C>G	ENSP00000486719.1:p.Thr949Ser
NM_000901.4:c.2834C>G	NP_000892.2:p.Thr945Ser
NM_001166104.1:c.2483C>G	NP_001159576.1:p.Thr828Ser
XM_011531975.1:c.2846C>G	XP_011530277.1:p.Thr949Ser
XM_011531976.1:c.2846C>G	XP_011530278.1:p.Thr949Ser
XM_011531977.1:c.2846C>G	XP_011530279.1:p.Thr949Ser
NM_001354819.1:c.2483C>G	NP_001341748.1:p.Thr828Ser
NR_148974.1:n.2701C>G
NM_000901.5:c.2834C>G MANE Select	NP_000892.2:p.Thr945Ser
NM_001166104.2:c.2483C>G	NP_001159576.1:p.Thr828Ser
NR_148974.2:n.2595C>G