Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19724181A>G , CM000684.2:g.19724181A>G | GRCh38 |
| NC_000022.10:g.19711704A>G , CM000684.1:g.19711704A>G | GRCh37 |
| NC_000022.9:g.18091704A>G | NCBI36 |
| NG_007974.1:g.5639A>G , LRG_478:g.5639A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000407.5:c.338A>G (GP1BB) MANE Select | NP_000398.1:p.Tyr113Cys |
| ENST00000366425.4:c.338A>G (GP1BB) MANE Select | ENSP00000383382.2:p.Tyr113Cys |
| NM_000407.4:c.338A>G , LRG_478t1:c.338A>G (GP1BB) | NP_000398.1:p.Tyr113Cys |
| NR_037611.1:n.4078A>G | |
| NR_037612.1:n.2582A>G | |
| ENST00000366425.3:c.338A>G (GP1BB) | ENSP00000383382.2:p.Tyr113Cys |
| ENST00000431044.5:c.*1423A>G (SEPTIN5) | ENSP00000399685.1:n.*1423A>G |
| ENST00000455843.5:c.*1423A>G (SEPTIN5) | ENSP00000391731.1:n.*1423A>G |
| ENST00000470814.1:n.2310A>G (SEPTIN5) |