Canonical Allele Identifier: CA804985127

Gene: NR3C1

Linked Data

• dbSNP Id: rs1463748684
• gnomAD v3: 5-143430518-A-G
• gnomAD v4: 5-143430518-A-G
• MyVariant Identifiers: chr5:g.142810083A>G (hg19) ; chr5:g.143430518A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143430518A>G , CM000667.2:g.143430518A>G	GRCh38
NC_000005.9:g.142810083A>G , CM000667.1:g.142810083A>G	GRCh37
NC_000005.8:g.142790276A>G	NCBI36
NG_009062.1:g.9995T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+4014T>C	ENSP00000343205.2:n.-14+4014T>C
ENST00000503701.1:n.352+3201T>C
ENST00000504572.5:c.-14+3201T>C	ENSP00000422518.1:n.-14+3201T>C
ENST00000505058.5:n.241+4014T>C
NM_001018074.1:c.-14+4686T>C	NP_001018084.1:n.-14+4686T>C
NM_001018075.1:c.-14+4783T>C	NP_001018085.1:n.-14+4783T>C
NM_001018077.1:c.-14+4014T>C	NP_001018087.1:n.-14+4014T>C
XM_005268422.2:c.-14+4014T>C	XP_005268479.1:n.-14+4014T>C
XM_005268422.3:c.-14+4014T>C	XP_005268479.1:n.-14+4014T>C
NM_001364183.1:c.-14+3201T>C	NP_001351112.1:n.-14+3201T>C
NM_001364183.2:c.-14+3201T>C	NP_001351112.1:n.-14+3201T>C