Canonical Allele Identifier: CA1502470298

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442486A= , CM000666.2:g.148442486A=	GRCh38
NC_000004.11:g.149363638A= , CM000666.1:g.149363638A=	GRCh37
NC_000004.10:g.149583088A=	NCBI36
NG_013350.1:g.5035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344721.8:c.-3+2040T=	ENSP00000341390.4:n.-3+2040T=
ENST00000358102.7:c.-329T=	ENSP00000350815.3:n.-329T=
ENST00000625323.2:c.-329T=	ENSP00000486719.1:n.-329T=
NM_000901.4:c.-329T=	NP_000892.2:n.-329T=
NM_001166104.1:c.-329T=	NP_001159576.1:n.-329T=
XM_011531975.1:c.-329T=	XP_011530277.1:n.-329T=
XM_011531976.1:c.-3+2040T=	XP_011530278.1:n.-3+2040T=
XM_011531977.1:c.-3+2714T=	XP_011530279.1:n.-3+2714T=
XM_011531978.1:c.-329T=	XP_011530280.1:n.-329T=
NM_001354819.1:c.-3+2040T=	NP_001341748.1:n.-3+2040T=
NR_148974.1:n.35T=
XM_011531978.2:c.-329T=	XP_011530280.1:n.-329T=