Canonical Allele Identifier: CA442002377

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148154804-T-G
• MyVariant Identifiers: chr4:g.149075955T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148154804T>G , CM000666.2:g.148154804T>G	GRCh38
NC_000004.11:g.149075955T>G , CM000666.1:g.149075955T>G	GRCh37
NC_000004.10:g.149295405T>G	NCBI36
NG_013350.1:g.292718A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2112A>C MANE Select	ENSP00000350815.3:p.Pro704=
ENST00000342437.8:c.2015-34516A>C	ENSP00000343907.4:n.2015-34516A>C
ENST00000344721.8:c.2112A>C	ENSP00000341390.4:p.Pro704=
ENST00000358102.7:c.2112A>C	ENSP00000350815.3:p.Pro704=
ENST00000503174.1:n.41A>C
ENST00000503313.1:n.309A>C
ENST00000511528.1:c.2124A>C	ENSP00000421481.1:p.Pro708=
ENST00000512865.5:c.2015-2191A>C	ENSP00000423510.1:n.2015-2191A>C
ENST00000625323.2:c.2124A>C	ENSP00000486719.1:p.Pro708=
NM_000901.4:c.2112A>C	NP_000892.2:p.Pro704=
NM_001166104.1:c.2015-2191A>C	NP_001159576.1:n.2015-2191A>C
XM_011531975.1:c.2124A>C	XP_011530277.1:p.Pro708=
XM_011531976.1:c.2124A>C	XP_011530278.1:p.Pro708=
XM_011531977.1:c.2124A>C	XP_011530279.1:p.Pro708=
XM_011531978.1:c.2124A>C	XP_011530280.1:p.Pro708=
NM_001354819.1:c.2015-2191A>C	NP_001341748.1:n.2015-2191A>C
NR_148974.1:n.2378-34516A>C
XM_011531978.2:c.2124A>C	XP_011530280.1:p.Pro708=
NM_000901.5:c.2112A>C MANE Select	NP_000892.2:p.Pro704=
NM_001166104.2:c.2015-2191A>C	NP_001159576.1:n.2015-2191A>C
NR_148974.2:n.2272-34516A>C