Linked Data
ClinVar Variation Id:
503498
ClinVar RCV Id:
RCV000594391
dbSNP Id:
rs770211260
ExAC:
7:23299717 T / G
gnomAD v2:
7-23299717-T-G
gnomAD v4:
7-23260098-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.23260098T>G , CM000669.2:g.23260098T>G | GRCh38 |
| NC_000007.13:g.23299717T>G , CM000669.1:g.23299717T>G | GRCh37 |
| NC_000007.12:g.23266242T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258733.9:c.660T>G MANE Select | ENSP00000258733.5:p.Tyr220Ter | |
| ENST00000647578.1:c.660T>G | ENSP00000497362.1:p.Tyr220Ter | |
| ENST00000258733.8:c.660T>G | ENSP00000258733.4:p.Tyr220Ter | |
| ENST00000381990.6:c.660T>G | ENSP00000371420.2:p.Tyr220Ter | |
| NM_001005340.1:c.660T>G | NP_001005340.1:p.Tyr220Ter | |
| NM_002510.2:c.660T>G | NP_002501.1:p.Tyr220Ter | |
| XM_005249578.1:c.660T>G | XP_005249635.1:p.Tyr220Ter | |
| XM_005249578.3:c.660T>G | XP_005249635.1:p.Tyr220Ter | |
| XM_017011676.2:c.660T>G | XP_016867165.1:p.Tyr220Ter | |
| XM_017011677.2:c.660T>G | XP_016867166.1:p.Tyr220Ter | |
| XM_017011678.2:c.660T>G | XP_016867167.1:p.Tyr220Ter | |
| NM_001005340.2:c.660T>G | NP_001005340.1:p.Tyr220Ter | |
| NM_002510.3:c.660T>G MANE Select | NP_002501.1:p.Tyr220Ter |