Canonical Allele Identifier: CA2672315346

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148442409-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442409T>C , CM000666.2:g.148442409T>C	GRCh38
NC_000004.11:g.149363561T>C , CM000666.1:g.149363561T>C	GRCh37
NC_000004.10:g.149583011T>C	NCBI36
NG_013350.1:g.5112A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.-252A>G MANE Select	ENSP00000350815.3:n.-252A>G
ENST00000344721.8:c.-3+2117A>G	ENSP00000341390.4:n.-3+2117A>G
ENST00000358102.7:c.-252A>G	ENSP00000350815.3:n.-252A>G
ENST00000625323.2:c.-252A>G	ENSP00000486719.1:n.-252A>G
NM_000901.4:c.-252A>G	NP_000892.2:n.-252A>G
NM_001166104.1:c.-252A>G	NP_001159576.1:n.-252A>G
XM_011531975.1:c.-252A>G	XP_011530277.1:n.-252A>G
XM_011531976.1:c.-3+2117A>G	XP_011530278.1:n.-3+2117A>G
XM_011531977.1:c.-3+2791A>G	XP_011530279.1:n.-3+2791A>G
XM_011531978.1:c.-252A>G	XP_011530280.1:n.-252A>G
NM_001354819.1:c.-3+2117A>G	NP_001341748.1:n.-3+2117A>G
NR_148974.1:n.112A>G
XM_011531978.2:c.-252A>G	XP_011530280.1:n.-252A>G
NM_000901.5:c.-252A>G MANE Select	NP_000892.2:n.-252A>G
NM_001166104.2:c.-252A>G	NP_001159576.1:n.-252A>G
NR_148974.2:n.6A>G