Canonical Allele Identifier: CA1082404576
Gene: NR3C1 HGNC NCBI

Linked Data

dbSNP Id: rs1841137008

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.143407047A>C , CM000667.2:g.143407047A>C GRCh38
NC_000005.9:g.142786612A>C , CM000667.1:g.142786612A>C GRCh37
NC_000005.8:g.142766805A>C NCBI36
NG_009062.1:g.33466T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343796.6:c.-13-6195T>G ENSP00000343205.2:n.-13-6195T>G
ENST00000504572.5:c.-13-6195T>G ENSP00000422518.1:n.-13-6195T>G
NM_001018074.1:c.-13-6195T>G NP_001018084.1:n.-13-6195T>G
NM_001018075.1:c.-13-6195T>G NP_001018085.1:n.-13-6195T>G
NM_001018077.1:c.-13-6195T>G NP_001018087.1:n.-13-6195T>G
XM_005268422.2:c.-13-6195T>G XP_005268479.1:n.-13-6195T>G
XM_005268422.3:c.-13-6195T>G XP_005268479.1:n.-13-6195T>G
NM_001364183.1:c.-13-6195T>G NP_001351112.1:n.-13-6195T>G
NM_001364183.2:c.-13-6195T>G NP_001351112.1:n.-13-6195T>G