Canonical Allele Identifier: CA2672314331

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148194999-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148194999T>A , CM000666.2:g.148194999T>A	GRCh38
NC_000004.11:g.149116150T>A , CM000666.1:g.149116150T>A	GRCh37
NC_000004.10:g.149335600T>A	NCBI36
NG_013350.1:g.252523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.1898-137A>T MANE Select	ENSP00000350815.3:n.1898-137A>T
ENST00000342437.8:c.1898-137A>T	ENSP00000343907.4:n.1898-137A>T
ENST00000344721.8:c.1898-137A>T	ENSP00000341390.4:n.1898-137A>T
ENST00000358102.7:c.1898-137A>T	ENSP00000350815.3:n.1898-137A>T
ENST00000503313.1:n.95-137A>T
ENST00000504753.1:n.347-137A>T
ENST00000511528.1:c.1910-137A>T	ENSP00000421481.1:n.1910-137A>T
ENST00000512865.5:c.1898-137A>T	ENSP00000423510.1:n.1898-137A>T
ENST00000625323.2:c.1910-137A>T	ENSP00000486719.1:n.1910-137A>T
NM_000901.4:c.1898-137A>T	NP_000892.2:n.1898-137A>T
NM_001166104.1:c.1898-137A>T	NP_001159576.1:n.1898-137A>T
XM_011531975.1:c.1910-137A>T	XP_011530277.1:n.1910-137A>T
XM_011531976.1:c.1910-137A>T	XP_011530278.1:n.1910-137A>T
XM_011531977.1:c.1910-137A>T	XP_011530279.1:n.1910-137A>T
XM_011531978.1:c.1910-137A>T	XP_011530280.1:n.1910-137A>T
NM_001354819.1:c.1898-137A>T	NP_001341748.1:n.1898-137A>T
NR_148974.1:n.2261-137A>T
XM_011531978.2:c.1910-137A>T	XP_011530280.1:n.1910-137A>T
NM_000901.5:c.1898-137A>T MANE Select	NP_000892.2:n.1898-137A>T
NM_001166104.2:c.1898-137A>T	NP_001159576.1:n.1898-137A>T
NR_148974.2:n.2155-137A>T