Linked Data
dbSNP Id:
rs755070825
ExAC:
17:40839855 C / A
gnomAD v2:
17-40839855-C-A
gnomAD v4:
17-42687837-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42687837C>A , CM000679.2:g.42687837C>A | GRCh38 |
| NC_000017.10:g.40839855C>A , CM000679.1:g.40839855C>A | GRCh37 |
| NC_000017.9:g.38093381C>A | NCBI36 |
| NG_042091.1:g.10224C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264638.9:c.1162C>A MANE Select | ENSP00000264638.3:p.Arg388Ser | |
| ENST00000264638.8:c.1162C>A | ENSP00000264638.3:p.Arg388Ser | |
| ENST00000586801.1:n.577C>A | ||
| ENST00000591662.1:c.1162C>A | ENSP00000466571.1:p.Arg388Ser | |
| NM_003632.2:c.1162C>A | NP_003623.1:p.Arg388Ser | |
| XM_005257748.3:c.934C>A | XP_005257805.1:p.Arg312Ser | |
| XM_005257748.4:c.934C>A | XP_005257805.1:p.Arg312Ser | |
| XM_017025238.1:c.1162C>A | XP_016880727.1:p.Arg388Ser | |
| XM_024451011.1:c.1162C>A | XP_024306779.1:p.Arg388Ser | |
| NM_003632.3:c.1162C>A MANE Select | NP_003623.1:p.Arg388Ser |