Linked Data
dbSNP Id:
rs754452405
ExAC:
17:4836920 T / C
gnomAD v2:
17-4836920-T-C
gnomAD v4:
17-4933625-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4933625T>C , CM000679.2:g.4933625T>C | GRCh38 |
| NC_000017.10:g.4836920T>C , CM000679.1:g.4836920T>C | GRCh37 |
| NC_000017.9:g.4777700T>C | NCBI36 |
| NG_008767.2:g.6331T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329125.6:c.1021T>C (GP1BA) MANE Select | ENSP00000329380.5:p.Ser341Pro | |
| ENST00000649830.1:c.-888+717A>G (CHRNE) | ENSP00000496907.1:n.-888+717A>G | |
| ENST00000329125.5:c.1021T>C (GP1BA) | ENSP00000329380.5:p.Ser341Pro | |
| ENST00000611961.1:c.1021T>C (GP1BA) | ENSP00000484439.1:p.Ser341Pro | |
| NM_000173.6:c.1021T>C (GP1BA) | NP_000164.5:p.Ser341Pro | |
| NM_000173.7:c.1021T>C (GP1BA) MANE Select | NP_000164.5:p.Ser341Pro |