Canonical Allele Identifier: CA2672315421

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148442463-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442463A>G , CM000666.2:g.148442463A>G	GRCh38
NC_000004.11:g.149363615A>G , CM000666.1:g.149363615A>G	GRCh37
NC_000004.10:g.149583065A>G	NCBI36
NG_013350.1:g.5058T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344721.8:c.-3+2063T>C	ENSP00000341390.4:n.-3+2063T>C
ENST00000358102.7:c.-306T>C	ENSP00000350815.3:n.-306T>C
ENST00000625323.2:c.-306T>C	ENSP00000486719.1:n.-306T>C
NM_000901.4:c.-306T>C	NP_000892.2:n.-306T>C
NM_001166104.1:c.-306T>C	NP_001159576.1:n.-306T>C
XM_011531975.1:c.-306T>C	XP_011530277.1:n.-306T>C
XM_011531976.1:c.-3+2063T>C	XP_011530278.1:n.-3+2063T>C
XM_011531977.1:c.-3+2737T>C	XP_011530279.1:n.-3+2737T>C
XM_011531978.1:c.-306T>C	XP_011530280.1:n.-306T>C
NM_001354819.1:c.-3+2063T>C	NP_001341748.1:n.-3+2063T>C
NR_148974.1:n.58T>C
XM_011531978.2:c.-306T>C	XP_011530280.1:n.-306T>C