Canonical Allele Identifier: CA1502460750

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148436882T= , CM000666.2:g.148436882T=	GRCh38
NC_000004.11:g.149358034T= , CM000666.1:g.149358034T=	GRCh37
NC_000004.10:g.149577484T=	NCBI36
NG_013350.1:g.10639A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.-2-20A= MANE Select	ENSP00000350815.3:n.-2-20A=
ENST00000342437.8:c.-2-20A=	ENSP00000343907.4:n.-2-20A=
ENST00000344721.8:c.-2-20A=	ENSP00000341390.4:n.-2-20A=
ENST00000358102.7:c.-2-20A=	ENSP00000350815.3:n.-2-20A=
ENST00000512865.5:c.-2-20A=	ENSP00000423510.1:n.-2-20A=
ENST00000625323.2:c.-2-20A=	ENSP00000486719.1:n.-2-20A=
NM_000901.4:c.-2-20A=	NP_000892.2:n.-2-20A=
NM_001166104.1:c.-2-20A=	NP_001159576.1:n.-2-20A=
XM_011531975.1:c.-2-20A=	XP_011530277.1:n.-2-20A=
XM_011531976.1:c.-2-20A=	XP_011530278.1:n.-2-20A=
XM_011531977.1:c.-2-20A=	XP_011530279.1:n.-2-20A=
XM_011531978.1:c.-2-20A=	XP_011530280.1:n.-2-20A=
NM_001354819.1:c.-2-20A=	NP_001341748.1:n.-2-20A=
NR_148974.1:n.362-20A=
XM_011531978.2:c.-2-20A=	XP_011530280.1:n.-2-20A=
NM_000901.5:c.-2-20A= MANE Select	NP_000892.2:n.-2-20A=
NM_001166104.2:c.-2-20A=	NP_001159576.1:n.-2-20A=
NR_148974.2:n.256-20A=