Canonical Allele Identifier: CA129267725

Gene: NR3C1

Linked Data

• dbSNP Id: rs988369266
• gnomAD v3: 5-143426394-A-G
• gnomAD v4: 5-143426394-A-G
• MyVariant Identifiers: chr5:g.142805959A>G (hg19) ; chr5:g.143426394A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426394A>G , CM000667.2:g.143426394A>G	GRCh38
NC_000005.9:g.142805959A>G , CM000667.1:g.142805959A>G	GRCh37
NC_000005.8:g.142786152A>G	NCBI36
NG_009062.1:g.14119T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8138T>C	ENSP00000343205.2:n.-14+8138T>C
ENST00000503701.1:n.352+7325T>C
ENST00000504572.5:c.-14+7325T>C	ENSP00000422518.1:n.-14+7325T>C
ENST00000505058.5:n.241+8138T>C
NM_001018074.1:c.-14+8810T>C	NP_001018084.1:n.-14+8810T>C
NM_001018075.1:c.-14+8907T>C	NP_001018085.1:n.-14+8907T>C
NM_001018077.1:c.-14+8138T>C	NP_001018087.1:n.-14+8138T>C
XM_005268422.2:c.-14+8138T>C	XP_005268479.1:n.-14+8138T>C
XM_005268422.3:c.-14+8138T>C	XP_005268479.1:n.-14+8138T>C
NM_001364183.1:c.-14+7325T>C	NP_001351112.1:n.-14+7325T>C
NM_001364183.2:c.-14+7325T>C	NP_001351112.1:n.-14+7325T>C