Canonical Allele Identifier: CA358250357

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149357937C>T (hg19) ; chr4:g.148436785C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148436785C>T , CM000666.2:g.148436785C>T	GRCh38
NC_000004.11:g.149357937C>T , CM000666.1:g.149357937C>T	GRCh37
NC_000004.10:g.149577387C>T	NCBI36
NG_013350.1:g.10736G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.76G>A MANE Select	ENSP00000350815.3:p.Val26Met
ENST00000342437.8:c.76G>A	ENSP00000343907.4:p.Val26Met
ENST00000344721.8:c.76G>A	ENSP00000341390.4:p.Val26Met
ENST00000358102.7:c.76G>A	ENSP00000350815.3:p.Val26Met
ENST00000511528.1:c.76G>A	ENSP00000421481.1:p.Val26Met
ENST00000512865.5:c.76G>A	ENSP00000423510.1:p.Val26Met
ENST00000625323.2:c.76G>A	ENSP00000486719.1:p.Val26Met
NM_000901.4:c.76G>A	NP_000892.2:p.Val26Met
NM_001166104.1:c.76G>A	NP_001159576.1:p.Val26Met
XM_011531975.1:c.76G>A	XP_011530277.1:p.Val26Met
XM_011531976.1:c.76G>A	XP_011530278.1:p.Val26Met
XM_011531977.1:c.76G>A	XP_011530279.1:p.Val26Met
XM_011531978.1:c.76G>A	XP_011530280.1:p.Val26Met
NM_001354819.1:c.76G>A	NP_001341748.1:p.Val26Met
NR_148974.1:n.439G>A
XM_011531978.2:c.76G>A	XP_011530280.1:p.Val26Met
NM_000901.5:c.76G>A MANE Select	NP_000892.2:p.Val26Met
NM_001166104.2:c.76G>A	NP_001159576.1:p.Val26Met
NR_148974.2:n.333G>A