Canonical Allele Identifier: CA129267729

Gene: NR3C1

Linked Data

• dbSNP Id: rs1047271906
• gnomAD v2: 5-142805998-A-G
• gnomAD v3: 5-143426433-A-G
• gnomAD v4: 5-143426433-A-G
• MyVariant Identifiers: chr5:g.142805998A>G (hg19) ; chr5:g.143426433A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426433A>G , CM000667.2:g.143426433A>G	GRCh38
NC_000005.9:g.142805998A>G , CM000667.1:g.142805998A>G	GRCh37
NC_000005.8:g.142786191A>G	NCBI36
NG_009062.1:g.14080T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8099T>C	ENSP00000343205.2:n.-14+8099T>C
ENST00000503701.1:n.352+7286T>C
ENST00000504572.5:c.-14+7286T>C	ENSP00000422518.1:n.-14+7286T>C
ENST00000505058.5:n.241+8099T>C
NM_001018074.1:c.-14+8771T>C	NP_001018084.1:n.-14+8771T>C
NM_001018075.1:c.-14+8868T>C	NP_001018085.1:n.-14+8868T>C
NM_001018077.1:c.-14+8099T>C	NP_001018087.1:n.-14+8099T>C
XM_005268422.2:c.-14+8099T>C	XP_005268479.1:n.-14+8099T>C
XM_005268422.3:c.-14+8099T>C	XP_005268479.1:n.-14+8099T>C
NM_001364183.1:c.-14+7286T>C	NP_001351112.1:n.-14+7286T>C
NM_001364183.2:c.-14+7286T>C	NP_001351112.1:n.-14+7286T>C