Canonical Allele Identifier: CA108477648

Gene: NR3C2

Linked Data

• dbSNP Id: rs967291389
• MyVariant Identifiers: chr4:g.149002432G>T (hg19) ; chr4:g.148081281G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081281G>T , CM000666.2:g.148081281G>T	GRCh38
NC_000004.11:g.149002432G>T , CM000666.1:g.149002432G>T	GRCh37
NC_000004.10:g.149221882G>T	NCBI36
NG_013350.1:g.366241C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.*63C>A MANE Select	ENSP00000350815.3:n.*63C>A
ENST00000342437.8:c.*401C>A	ENSP00000343907.4:n.*401C>A
ENST00000344721.8:c.*63C>A	ENSP00000341390.4:n.*63C>A
ENST00000358102.7:c.*63C>A	ENSP00000350815.3:n.*63C>A
ENST00000512865.5:c.*63C>A	ENSP00000423510.1:n.*63C>A
ENST00000625323.2:c.*63C>A	ENSP00000486719.1:n.*63C>A
NM_000901.4:c.*63C>A	NP_000892.2:n.*63C>A
NM_001166104.1:c.*63C>A	NP_001159576.1:n.*63C>A
XM_011531975.1:c.*63C>A	XP_011530277.1:n.*63C>A
XM_011531976.1:c.*63C>A	XP_011530278.1:n.*63C>A
XM_011531977.1:c.*63C>A	XP_011530279.1:n.*63C>A
NM_001354819.1:c.*63C>A	NP_001341748.1:n.*63C>A
NR_148974.1:n.2885C>A
NM_000901.5:c.*63C>A MANE Select	NP_000892.2:n.*63C>A
NM_001166104.2:c.*63C>A	NP_001159576.1:n.*63C>A
NR_148974.2:n.2779C>A