Linked Data
dbSNP Id:
rs1459040516
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1014032T>C , CM000663.2:g.1014032T>C | GRCh38 |
| NC_000001.10:g.949412T>C , CM000663.1:g.949412T>C | GRCh37 |
| NC_000001.9:g.939275T>C | NCBI36 |
| NG_033033.1:g.5566T>C | |
| NG_033033.2:g.17895T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000624697.4:c.28T>C | ENSP00000485643.1:p.Ser10Pro | |
| ENST00000649529.1:c.52T>C MANE Select | ENSP00000496832.1:p.Ser18Pro | |
| ENST00000379389.4:c.52T>C | ENSP00000368699.4:p.Ser18Pro | |
| ENST00000624652.1:c.28T>C | ENSP00000485313.1:p.Ser10Pro | |
| ENST00000624697.3:c.28T>C | ENSP00000485643.1:p.Ser10Pro | |
| NM_005101.3:c.52T>C | NP_005092.1:p.Ser18Pro | |
| NM_005101.4:c.52T>C MANE Select | NP_005092.1:p.Ser18Pro |