Canonical Allele Identifier: CA804974807

Gene: NR3C1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143407169C>T , CM000667.2:g.143407169C>T	GRCh38
NC_000005.9:g.142786734C>T , CM000667.1:g.142786734C>T	GRCh37
NC_000005.8:g.142766927C>T	NCBI36
NG_009062.1:g.33344G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-13-6317G>A	ENSP00000343205.2:n.-13-6317G>A
ENST00000504572.5:c.-13-6317G>A	ENSP00000422518.1:n.-13-6317G>A
NM_001018074.1:c.-13-6317G>A	NP_001018084.1:n.-13-6317G>A
NM_001018075.1:c.-13-6317G>A	NP_001018085.1:n.-13-6317G>A
NM_001018077.1:c.-13-6317G>A	NP_001018087.1:n.-13-6317G>A
XM_005268422.2:c.-13-6317G>A	XP_005268479.1:n.-13-6317G>A
XM_005268422.3:c.-13-6317G>A	XP_005268479.1:n.-13-6317G>A
NM_001364183.1:c.-13-6317G>A	NP_001351112.1:n.-13-6317G>A
NM_001364183.2:c.-13-6317G>A	NP_001351112.1:n.-13-6317G>A