Canonical Allele Identifier: CA129267719

Gene: NR3C1

Linked Data

• dbSNP Id: rs561978230
• gnomAD v3: 5-143426316-A-C
• gnomAD v4: 5-143426316-A-C
• MyVariant Identifiers: chr5:g.142805881A>C (hg19) ; chr5:g.143426316A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426316A>C , CM000667.2:g.143426316A>C	GRCh38
NC_000005.9:g.142805881A>C , CM000667.1:g.142805881A>C	GRCh37
NC_000005.8:g.142786074A>C	NCBI36
NG_009062.1:g.14197T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8216T>G	ENSP00000343205.2:n.-14+8216T>G
ENST00000503701.1:n.352+7403T>G
ENST00000504572.5:c.-14+7403T>G	ENSP00000422518.1:n.-14+7403T>G
ENST00000505058.5:n.241+8216T>G
NM_001018074.1:c.-14+8888T>G	NP_001018084.1:n.-14+8888T>G
NM_001018075.1:c.-14+8985T>G	NP_001018085.1:n.-14+8985T>G
NM_001018077.1:c.-14+8216T>G	NP_001018087.1:n.-14+8216T>G
XM_005268422.2:c.-14+8216T>G	XP_005268479.1:n.-14+8216T>G
XM_005268422.3:c.-14+8216T>G	XP_005268479.1:n.-14+8216T>G
NM_001364183.1:c.-14+7403T>G	NP_001351112.1:n.-14+7403T>G
NM_001364183.2:c.-14+7403T>G	NP_001351112.1:n.-14+7403T>G