Canonical Allele Identifier: CA129265767

Gene: NR3C1

Linked Data

• dbSNP Id: rs922987144
• MyVariant Identifiers: chr5:g.142786564A>G (hg19) ; chr5:g.143406999A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.143406999A>G , CM000667.2:g.143406999A>G	GRCh38
NC_000005.9:g.142786564A>G , CM000667.1:g.142786564A>G	GRCh37
NC_000005.8:g.142766757A>G	NCBI36
NG_009062.1:g.33514T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343796.6:c.-13-6147T>C	ENSP00000343205.2:n.-13-6147T>C
ENST00000504572.5:c.-13-6147T>C	ENSP00000422518.1:n.-13-6147T>C
NM_001018074.1:c.-13-6147T>C	NP_001018084.1:n.-13-6147T>C
NM_001018075.1:c.-13-6147T>C	NP_001018085.1:n.-13-6147T>C
NM_001018077.1:c.-13-6147T>C	NP_001018087.1:n.-13-6147T>C
XM_005268422.2:c.-13-6147T>C	XP_005268479.1:n.-13-6147T>C
XM_005268422.3:c.-13-6147T>C	XP_005268479.1:n.-13-6147T>C
NM_001364183.1:c.-13-6147T>C	NP_001351112.1:n.-13-6147T>C
NM_001364183.2:c.-13-6147T>C	NP_001351112.1:n.-13-6147T>C