Canonical Allele Identifier: CA1502331275

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081285T= , CM000666.2:g.148081285T=	GRCh38
NC_000004.11:g.149002436T= , CM000666.1:g.149002436T=	GRCh37
NC_000004.10:g.149221886T=	NCBI36
NG_013350.1:g.366237A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.*59A= MANE Select	ENSP00000350815.3:n.*59A=
ENST00000342437.8:c.*397A=	ENSP00000343907.4:n.*397A=
ENST00000344721.8:c.*59A=	ENSP00000341390.4:n.*59A=
ENST00000358102.7:c.*59A=	ENSP00000350815.3:n.*59A=
ENST00000512865.5:c.*59A=	ENSP00000423510.1:n.*59A=
ENST00000625323.2:c.*59A=	ENSP00000486719.1:n.*59A=
NM_000901.4:c.*59A=	NP_000892.2:n.*59A=
NM_001166104.1:c.*59A=	NP_001159576.1:n.*59A=
XM_011531975.1:c.*59A=	XP_011530277.1:n.*59A=
XM_011531976.1:c.*59A=	XP_011530278.1:n.*59A=
XM_011531977.1:c.*59A=	XP_011530279.1:n.*59A=
NM_001354819.1:c.*59A=	NP_001341748.1:n.*59A=
NR_148974.1:n.2881A=
NM_000901.5:c.*59A= MANE Select	NP_000892.2:n.*59A=
NM_001166104.2:c.*59A=	NP_001159576.1:n.*59A=
NR_148974.2:n.2775A=