Canonical Allele Identifier: CA788847301

Gene: NR3C2

Linked Data

• dbSNP Id: rs1301825039
• gnomAD v3: 4-148442468-G-A
• gnomAD v4: 4-148442468-G-A
• MyVariant Identifiers: chr4:g.149363620G>A (hg19) ; chr4:g.148442468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442468G>A , CM000666.2:g.148442468G>A	GRCh38
NC_000004.11:g.149363620G>A , CM000666.1:g.149363620G>A	GRCh37
NC_000004.10:g.149583070G>A	NCBI36
NG_013350.1:g.5053C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344721.8:c.-3+2058C>T	ENSP00000341390.4:n.-3+2058C>T
ENST00000358102.7:c.-311C>T	ENSP00000350815.3:n.-311C>T
ENST00000625323.2:c.-311C>T	ENSP00000486719.1:n.-311C>T
NM_000901.4:c.-311C>T	NP_000892.2:n.-311C>T
NM_001166104.1:c.-311C>T	NP_001159576.1:n.-311C>T
XM_011531975.1:c.-311C>T	XP_011530277.1:n.-311C>T
XM_011531976.1:c.-3+2058C>T	XP_011530278.1:n.-3+2058C>T
XM_011531977.1:c.-3+2732C>T	XP_011530279.1:n.-3+2732C>T
XM_011531978.1:c.-311C>T	XP_011530280.1:n.-311C>T
NM_001354819.1:c.-3+2058C>T	NP_001341748.1:n.-3+2058C>T
NR_148974.1:n.53C>T
XM_011531978.2:c.-311C>T	XP_011530280.1:n.-311C>T