Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19724072G>A , CM000684.2:g.19724072G>A | GRCh38 |
| NC_000022.10:g.19711595G>A , CM000684.1:g.19711595G>A | GRCh37 |
| NC_000022.9:g.18091595G>A | NCBI36 |
| NG_007974.1:g.5530G>A , LRG_478:g.5530G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366425.4:c.229G>A (GP1BB) MANE Select | ENSP00000383382.2:p.Ala77Thr | |
| ENST00000366425.3:c.229G>A (GP1BB) | ENSP00000383382.2:p.Ala77Thr | |
| ENST00000431044.5:c.*1314G>A (SEPTIN5) | ENSP00000399685.1:n.*1314G>A | |
| ENST00000455843.5:c.*1314G>A (SEPTIN5) | ENSP00000391731.1:n.*1314G>A | |
| ENST00000470814.1:n.2201G>A (SEPTIN5) | ||
| NM_000407.4:c.229G>A , LRG_478t1:c.229G>A (GP1BB) | NP_000398.1:p.Ala77Thr | |
| NR_037611.1:n.3969G>A | ||
| NR_037612.1:n.2473G>A | ||
| NM_000407.5:c.229G>A (GP1BB) MANE Select | NP_000398.1:p.Ala77Thr |