Canonical Allele Identifier: CA3100541
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 256827
dbSNP Id: rs2070951

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148436862G>C , CM000666.2:g.148436862G>C GRCh38
NC_000004.11:g.149358014G>C , CM000666.1:g.149358014G>C GRCh37
NC_000004.10:g.149577464G>C NCBI36
NG_013350.1:g.10659C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000358102.8:c.-2C>G MANE Select ENSP00000350815.3:p.=
ENST00000342437.8:c.-2C>G ENSP00000343907.4:p.=
ENST00000344721.8:c.-2C>G ENSP00000341390.4:p.=
ENST00000358102.7:c.-2C>G ENSP00000350815.3:p.=
ENST00000512865.5:c.-2C>G ENSP00000423510.1:p.=
ENST00000625323.2:c.-2C>G ENSP00000486719.1:p.=
NM_000901.4:c.-2C>G NP_000892.2:p.=
NM_001166104.1:c.-2C>G NP_001159576.1:p.=
XM_011531975.1:c.-2C>G XP_011530277.1:p.=
XM_011531976.1:c.-2C>G XP_011530278.1:p.=
XM_011531977.1:c.-2C>G XP_011530279.1:p.=
XM_011531978.1:c.-2C>G XP_011530280.1:p.=
NM_001354819.1:c.-2C>G NP_001341748.1:p.=
NR_148974.1:n.362C>G
XM_011531978.2:c.-2C>G XP_011530280.1:p.=
NM_000901.5:c.-2C>G MANE Select NP_000892.2:p.=
NM_001166104.2:c.-2C>G NP_001159576.1:p.=
NR_148974.2:n.256C>G