Canonical Allele Identifier: CA129267732

Gene: NR3C1

Linked Data

• dbSNP Id: rs918094463
• MyVariant Identifiers: chr5:g.142806018A>T (hg19) ; chr5:g.143426453A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143426453A>T , CM000667.2:g.143426453A>T	GRCh38
NC_000005.9:g.142806018A>T , CM000667.1:g.142806018A>T	GRCh37
NC_000005.8:g.142786211A>T	NCBI36
NG_009062.1:g.14060T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-14+8079T>A	ENSP00000343205.2:n.-14+8079T>A
ENST00000503701.1:n.352+7266T>A
ENST00000504572.5:c.-14+7266T>A	ENSP00000422518.1:n.-14+7266T>A
ENST00000505058.5:n.241+8079T>A
NM_001018074.1:c.-14+8751T>A	NP_001018084.1:n.-14+8751T>A
NM_001018075.1:c.-14+8848T>A	NP_001018085.1:n.-14+8848T>A
NM_001018077.1:c.-14+8079T>A	NP_001018087.1:n.-14+8079T>A
XM_005268422.2:c.-14+8079T>A	XP_005268479.1:n.-14+8079T>A
XM_005268422.3:c.-14+8079T>A	XP_005268479.1:n.-14+8079T>A
NM_001364183.1:c.-14+7266T>A	NP_001351112.1:n.-14+7266T>A
NM_001364183.2:c.-14+7266T>A	NP_001351112.1:n.-14+7266T>A