Linked Data
dbSNP Id:
rs545055627
ExAC:
7:75614055 C / T
gnomAD v2:
7-75614055-C-T
gnomAD v3:
7-75984737-C-T
gnomAD v4:
7-75984737-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.75984737C>T , CM000669.2:g.75984737C>T | GRCh38 |
| NC_000007.13:g.75614055C>T , CM000669.1:g.75614055C>T | GRCh37 |
| NC_000007.12:g.75451991C>T | NCBI36 |
| NG_008930.1:g.74636C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475509.2:c.842-40C>T | ENSP00000516446.1:n.842-40C>T | |
| ENST00000706544.1:c.968-40C>T | ENSP00000516442.1:n.968-40C>T | |
| ENST00000706545.1:c.1067-40C>T | ENSP00000516443.1:n.1067-40C>T | |
| ENST00000706546.1:c.1067-40C>T | ENSP00000516444.1:n.1067-40C>T | |
| ENST00000706547.1:c.1067-40C>T | ENSP00000516445.1:n.1067-40C>T | |
| ENST00000461988.6:c.1067-40C>T MANE Select | ENSP00000419970.1:n.1067-40C>T | |
| ENST00000394893.5:c.1067-40C>T | ENSP00000378355.1:n.1067-40C>T | |
| ENST00000412064.6:c.*108+1101C>T | ENSP00000404731.2:n.*108+1101C>T | |
| ENST00000439269.1:c.281-40C>T | ENSP00000412490.1:n.281-40C>T | |
| ENST00000447222.5:c.1218-40C>T | ||
| ENST00000454934.5:c.*372-40C>T | ENSP00000414263.1:n.*372-40C>T | |
| ENST00000461988.5:c.1067-40C>T | ENSP00000419970.1:n.1067-40C>T | |
| ENST00000487247.5:n.422-40C>T | ||
| ENST00000495770.1:n.69-40C>T | ||
| ENST00000496888.5:n.441-40C>T | ||
| NM_000941.2:c.1067-40C>T | NP_000932.3:n.1067-40C>T | |
| NM_000941.3:c.1067-40C>T | NP_000932.3:n.1067-40C>T | |
| NM_001367562.1:c.1067-40C>T | NP_001354491.1:n.1067-40C>T | |
| NM_001382655.1:c.1121-40C>T | NP_001369584.1:n.1121-40C>T | |
| NM_001382657.1:c.1067-40C>T | NP_001369586.1:n.1067-40C>T | |
| NM_001382658.1:c.1067-40C>T | NP_001369587.1:n.1067-40C>T | |
| NM_001382659.1:c.1067-40C>T | NP_001369588.1:n.1067-40C>T | |
| NM_001382662.1:c.1067-40C>T | NP_001369591.1:n.1067-40C>T | |
| NM_001367562.3:c.1058-40C>T | NP_001354491.2:n.1058-40C>T | |
| NM_001382655.3:c.1112-40C>T | NP_001369584.2:n.1112-40C>T | |
| NM_001382657.2:c.1058-40C>T | NP_001369586.2:n.1058-40C>T | |
| NM_001382658.3:c.1058-40C>T | NP_001369587.2:n.1058-40C>T | |
| NM_001382659.3:c.1058-40C>T | NP_001369588.2:n.1058-40C>T | |
| NM_001382662.3:c.1058-40C>T | NP_001369591.2:n.1058-40C>T | |
| NM_001395413.1:c.1058-40C>T MANE Select | NP_001382342.1:n.1058-40C>T |