Canonical Allele Identifier: CA2672312783

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148081176-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081176G>A , CM000666.2:g.148081176G>A	GRCh38
NC_000004.11:g.149002327G>A , CM000666.1:g.149002327G>A	GRCh37
NC_000004.10:g.149221777G>A	NCBI36
NG_013350.1:g.366346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.*168C>T MANE Select	ENSP00000350815.3:n.*168C>T
ENST00000342437.8:c.*506C>T	ENSP00000343907.4:n.*506C>T
ENST00000344721.8:c.*168C>T	ENSP00000341390.4:n.*168C>T
ENST00000358102.7:c.*168C>T	ENSP00000350815.3:n.*168C>T
ENST00000512865.5:c.*168C>T	ENSP00000423510.1:n.*168C>T
ENST00000625323.2:c.*168C>T	ENSP00000486719.1:n.*168C>T
NM_000901.4:c.*168C>T	NP_000892.2:n.*168C>T
NM_001166104.1:c.*168C>T	NP_001159576.1:n.*168C>T
XM_011531975.1:c.*168C>T	XP_011530277.1:n.*168C>T
XM_011531976.1:c.*168C>T	XP_011530278.1:n.*168C>T
XM_011531977.1:c.*168C>T	XP_011530279.1:n.*168C>T
NM_001354819.1:c.*168C>T	NP_001341748.1:n.*168C>T
NR_148974.1:n.2990C>T
NM_000901.5:c.*168C>T MANE Select	NP_000892.2:n.*168C>T
NM_001166104.2:c.*168C>T	NP_001159576.1:n.*168C>T
NR_148974.2:n.2884C>T