Linked Data
dbSNP Id:
rs1782240229
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131877159T>C , CM000668.2:g.131877159T>C | GRCh38 |
| NC_000006.11:g.132198299T>C , CM000668.1:g.132198299T>C | GRCh37 |
| NC_000006.10:g.132239992T>C | NCBI36 |
| NG_008206.1:g.74144T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683687.1:n.763T>C | ||
| ENST00000684536.1:n.389T>C | ||
| ENST00000647893.1:c.1891T>C MANE Select | ENSP00000498074.1:p.Ser631Pro | |
| ENST00000647981.1:n.576T>C | ||
| ENST00000650437.1:c.1382T>C | ||
| ENST00000360971.6:c.1891T>C | ENSP00000354238.2:p.Ser631Pro | |
| ENST00000459624.1:n.935T>C | ||
| ENST00000513998.5:c.*728T>C | ENSP00000422424.1:n.*728T>C | |
| NM_006208.2:c.1891T>C | NP_006199.2:p.Ser631Pro | |
| XM_011535896.1:c.781T>C | XP_011534198.1:p.Ser261Pro | |
| NM_006208.3:c.1891T>C MANE Select | NP_006199.2:p.Ser631Pro |