Canonical Allele Identifier: CA2578208168

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148081265-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081265A>G , CM000666.2:g.148081265A>G	GRCh38
NC_000004.11:g.149002416A>G , CM000666.1:g.149002416A>G	GRCh37
NC_000004.10:g.149221866A>G	NCBI36
NG_013350.1:g.366257T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.*79T>C MANE Select	ENSP00000350815.3:n.*79T>C
ENST00000342437.8:c.*417T>C	ENSP00000343907.4:n.*417T>C
ENST00000344721.8:c.*79T>C	ENSP00000341390.4:n.*79T>C
ENST00000358102.7:c.*79T>C	ENSP00000350815.3:n.*79T>C
ENST00000512865.5:c.*79T>C	ENSP00000423510.1:n.*79T>C
ENST00000625323.2:c.*79T>C	ENSP00000486719.1:n.*79T>C
NM_000901.4:c.*79T>C	NP_000892.2:n.*79T>C
NM_001166104.1:c.*79T>C	NP_001159576.1:n.*79T>C
XM_011531975.1:c.*79T>C	XP_011530277.1:n.*79T>C
XM_011531976.1:c.*79T>C	XP_011530278.1:n.*79T>C
XM_011531977.1:c.*79T>C	XP_011530279.1:n.*79T>C
NM_001354819.1:c.*79T>C	NP_001341748.1:n.*79T>C
NR_148974.1:n.2901T>C
NM_000901.5:c.*79T>C MANE Select	NP_000892.2:n.*79T>C
NM_001166104.2:c.*79T>C	NP_001159576.1:n.*79T>C
NR_148974.2:n.2795T>C