Linked Data
ClinVar Variation Id:
1617276
ClinVar RCV Id:
RCV002076486
dbSNP Id:
rs2135842913
COSMIC:
COSM5545684
MyVariant Identifiers:
chr11:g.64527344C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64759872C>T , CM000673.2:g.64759872C>T | GRCh38 |
| NC_000011.9:g.64527344C>T , CM000673.1:g.64527344C>T | GRCh37 |
| NC_000011.8:g.64283920C>T | NCBI36 |
| NG_013018.1:g.5844G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000164139.4:c.27G>A MANE Select | ENSP00000164139.3:p.Glu9= | |
| ENST00000164139.3:c.27G>A | ENSP00000164139.3:p.Glu9= | |
| ENST00000377432.7:c.27G>A | ENSP00000366650.3:p.Glu9= | |
| NM_001164716.1:c.27G>A | NP_001158188.1:p.Glu9= | |
| NM_005609.2:c.27G>A | NP_005600.1:p.Glu9= | |
| NM_005609.3:c.27G>A | NP_005600.1:p.Glu9= | |
| NM_005609.4:c.27G>A MANE Select | NP_005600.1:p.Glu9= |