Canonical Allele Identifier: CA1502470021

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442406G= , CM000666.2:g.148442406G=	GRCh38
NC_000004.11:g.149363558G= , CM000666.1:g.149363558G=	GRCh37
NC_000004.10:g.149583008G=	NCBI36
NG_013350.1:g.5115C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.-249C= MANE Select	ENSP00000350815.3:n.-249C=
ENST00000344721.8:c.-3+2120C=	ENSP00000341390.4:n.-3+2120C=
ENST00000358102.7:c.-249C=	ENSP00000350815.3:n.-249C=
ENST00000625323.2:c.-249C=	ENSP00000486719.1:n.-249C=
NM_000901.4:c.-249C=	NP_000892.2:n.-249C=
NM_001166104.1:c.-249C=	NP_001159576.1:n.-249C=
XM_011531975.1:c.-249C=	XP_011530277.1:n.-249C=
XM_011531976.1:c.-3+2120C=	XP_011530278.1:n.-3+2120C=
XM_011531977.1:c.-3+2794C=	XP_011530279.1:n.-3+2794C=
XM_011531978.1:c.-249C=	XP_011530280.1:n.-249C=
NM_001354819.1:c.-3+2120C=	NP_001341748.1:n.-3+2120C=
NR_148974.1:n.115C=
XM_011531978.2:c.-249C=	XP_011530280.1:n.-249C=
NM_000901.5:c.-249C= MANE Select	NP_000892.2:n.-249C=
NM_001166104.2:c.-249C=	NP_001159576.1:n.-249C=
NR_148974.2:n.9C=