Linked Data
ClinVar Variation Id:
194358
dbSNP Id:
rs794727120
gnomAD v4:
6-64997647-G-A
COSMIC:
COSM4910213
PubMed:
PMID:23891399
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.64997647G>A , CM000668.2:g.64997647G>A | GRCh38 |
| NC_000006.11:g.65707540G>A , CM000668.1:g.65707540G>A | GRCh37 |
| NC_000006.10:g.65764261G>A | NCBI36 |
| NG_023443.1:g.714579C>T | |
| NG_023443.2:g.714579C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503581.6:c.2194C>T MANE Select | ENSP00000424243.1:p.Gln732Ter | |
| ENST00000370616.6:c.2194C>T | ENSP00000359650.2:p.Gln732Ter | |
| ENST00000370618.7:c.2194C>T | ENSP00000359652.4:p.Gln732Ter | |
| ENST00000370621.7:c.2194C>T | ENSP00000359655.3:p.Gln732Ter | |
| ENST00000503581.5:c.2194C>T | ENSP00000424243.1:p.Gln732Ter | |
| NM_001142800.1:c.2194C>T | NP_001136272.1:p.Gln732Ter | |
| NM_001292009.1:c.2194C>T | NP_001278938.1:p.Gln732Ter | |
| NM_001142800.2:c.2194C>T MANE Select | NP_001136272.1:p.Gln732Ter | |
| NM_001292009.2:c.2194C>T | NP_001278938.1:p.Gln732Ter |