Canonical Allele Identifier: CA1502381468

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154526C= , CM000666.2:g.148154526C=	GRCh38
NC_000004.11:g.149075677C= , CM000666.1:g.149075677C=	GRCh37
NC_000004.10:g.149295127C=	NCBI36
NG_013350.1:g.292996G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2365+25G= MANE Select	ENSP00000350815.3:n.2365+25G=
ENST00000342437.8:c.2015-34238G=	ENSP00000343907.4:n.2015-34238G=
ENST00000344721.8:c.2365+25G=	ENSP00000341390.4:n.2365+25G=
ENST00000358102.7:c.2365+25G=	ENSP00000350815.3:n.2365+25G=
ENST00000503174.1:n.294+25G=
ENST00000503313.1:n.562+25G=
ENST00000511528.1:c.2377+25G=	ENSP00000421481.1:n.2377+25G=
ENST00000512865.5:c.2015-1913G=	ENSP00000423510.1:n.2015-1913G=
ENST00000625323.2:c.2377+25G=	ENSP00000486719.1:n.2377+25G=
NM_000901.4:c.2365+25G=	NP_000892.2:n.2365+25G=
NM_001166104.1:c.2015-1913G=	NP_001159576.1:n.2015-1913G=
XM_011531975.1:c.2377+25G=	XP_011530277.1:n.2377+25G=
XM_011531976.1:c.2377+25G=	XP_011530278.1:n.2377+25G=
XM_011531977.1:c.2377+25G=	XP_011530279.1:n.2377+25G=
XM_011531978.1:c.2377+25G=	XP_011530280.1:n.2377+25G=
NM_001354819.1:c.2015-1913G=	NP_001341748.1:n.2015-1913G=
NR_148974.1:n.2378-34238G=
XM_011531978.2:c.2377+25G=	XP_011530280.1:n.2377+25G=
NM_000901.5:c.2365+25G= MANE Select	NP_000892.2:n.2365+25G=
NM_001166104.2:c.2015-1913G=	NP_001159576.1:n.2015-1913G=
NR_148974.2:n.2272-34238G=