Canonical Allele Identifier: CA1502333645

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154892G= , CM000666.2:g.148154892G=	GRCh38
NC_000004.11:g.149076043G= , CM000666.1:g.149076043G=	GRCh37
NC_000004.10:g.149295493G=	NCBI36
NG_013350.1:g.292630C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000901.5:c.2024C= MANE Select	NP_000892.2:p.Ser675=
ENST00000358102.8:c.2024C= MANE Select	ENSP00000350815.3:p.Ser675=
NM_000901.4:c.2024C=	NP_000892.2:p.Ser675=
NM_001166104.1:c.2015-2279C=	NP_001159576.1:n.2015-2279C=
NM_001166104.2:c.2015-2279C=	NP_001159576.1:n.2015-2279C=
NM_001354819.1:c.2015-2279C=	NP_001341748.1:n.2015-2279C=
NR_148974.1:n.2378-34604C=
NR_148974.2:n.2272-34604C=
ENST00000342437.8:c.2015-34604C=	ENSP00000343907.4:n.2015-34604C=
ENST00000344721.8:c.2024C=	ENSP00000341390.4:p.Ser675=
ENST00000358102.7:c.2024C=	ENSP00000350815.3:p.Ser675=
ENST00000503313.1:n.221C=
ENST00000511528.1:c.2036C=	ENSP00000421481.1:p.Ser679=
ENST00000512865.5:c.2015-2279C=	ENSP00000423510.1:n.2015-2279C=
ENST00000625323.2:c.2036C=	ENSP00000486719.1:p.Ser679=
XM_011531975.1:c.2036C=	XP_011530277.1:p.Ser679=
XM_011531976.1:c.2036C=	XP_011530278.1:p.Ser679=
XM_011531977.1:c.2036C=	XP_011530279.1:p.Ser679=
XM_011531978.1:c.2036C=	XP_011530280.1:p.Ser679=
XM_011531978.2:c.2036C=	XP_011530280.1:p.Ser679=