Canonical Allele Identifier: CA788777521

Gene: NR3C2

Linked Data

• dbSNP Id: rs975825425
• gnomAD v3: 4-148152416-A-C
• gnomAD v4: 4-148152416-A-C
• MyVariant Identifiers: chr4:g.149073567A>C (hg19) ; chr4:g.148152416A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152416A>C , CM000666.2:g.148152416A>C	GRCh38
NC_000004.11:g.149073567A>C , CM000666.1:g.149073567A>C	GRCh37
NC_000004.10:g.149293017A>C	NCBI36
NG_013350.1:g.295106T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2510+53T>G MANE Select	ENSP00000350815.3:n.2510+53T>G
ENST00000342437.8:c.2015-32128T>G	ENSP00000343907.4:n.2015-32128T>G
ENST00000344721.8:c.2510+53T>G	ENSP00000341390.4:n.2510+53T>G
ENST00000358102.7:c.2510+53T>G	ENSP00000350815.3:n.2510+53T>G
ENST00000503313.1:n.707+53T>G
ENST00000511528.1:c.2522+53T>G	ENSP00000421481.1:n.2522+53T>G
ENST00000512865.5:c.2159+53T>G	ENSP00000423510.1:n.2159+53T>G
ENST00000625323.2:c.2522+53T>G	ENSP00000486719.1:n.2522+53T>G
NM_000901.4:c.2510+53T>G	NP_000892.2:n.2510+53T>G
NM_001166104.1:c.2159+53T>G	NP_001159576.1:n.2159+53T>G
XM_011531975.1:c.2522+53T>G	XP_011530277.1:n.2522+53T>G
XM_011531976.1:c.2522+53T>G	XP_011530278.1:n.2522+53T>G
XM_011531977.1:c.2522+53T>G	XP_011530279.1:n.2522+53T>G
XM_011531978.1:c.2522+53T>G	XP_011530280.1:n.2522+53T>G
NM_001354819.1:c.2159+53T>G	NP_001341748.1:n.2159+53T>G
NR_148974.1:n.2378-32128T>G
XM_011531978.2:c.2522+53T>G	XP_011530280.1:n.2522+53T>G
NM_000901.5:c.2510+53T>G MANE Select	NP_000892.2:n.2510+53T>G
NM_001166104.2:c.2159+53T>G	NP_001159576.1:n.2159+53T>G
NR_148974.2:n.2272-32128T>G