Canonical Allele Identifier: CA1082404589

Gene: NR3C1

Linked Data

• dbSNP Id: rs1841138701
• gnomAD v3: 5-143407096-A-C
• gnomAD v4: 5-143407096-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143407096A>C , CM000667.2:g.143407096A>C	GRCh38
NC_000005.9:g.142786661A>C , CM000667.1:g.142786661A>C	GRCh37
NC_000005.8:g.142766854A>C	NCBI36
NG_009062.1:g.33417T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000343796.6:c.-13-6244T>G	ENSP00000343205.2:n.-13-6244T>G
ENST00000504572.5:c.-13-6244T>G	ENSP00000422518.1:n.-13-6244T>G
NM_001018074.1:c.-13-6244T>G	NP_001018084.1:n.-13-6244T>G
NM_001018075.1:c.-13-6244T>G	NP_001018085.1:n.-13-6244T>G
NM_001018077.1:c.-13-6244T>G	NP_001018087.1:n.-13-6244T>G
XM_005268422.2:c.-13-6244T>G	XP_005268479.1:n.-13-6244T>G
XM_005268422.3:c.-13-6244T>G	XP_005268479.1:n.-13-6244T>G
NM_001364183.1:c.-13-6244T>G	NP_001351112.1:n.-13-6244T>G
NM_001364183.2:c.-13-6244T>G	NP_001351112.1:n.-13-6244T>G