Linked Data
MyVariant Identifiers:
chr22:g.19711435C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19723912C>A , CM000684.2:g.19723912C>A | GRCh38 |
| NC_000022.10:g.19711435C>A , CM000684.1:g.19711435C>A | GRCh37 |
| NC_000022.9:g.18091435C>A | NCBI36 |
| NG_007974.1:g.5370C>A , LRG_478:g.5370C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366425.4:c.69C>A (GP1BB) MANE Select | ENSP00000383382.2:p.Ala23= | |
| ENST00000366425.3:c.69C>A (GP1BB) | ENSP00000383382.2:p.Ala23= | |
| ENST00000431044.5:c.*1154C>A (SEPTIN5) | ENSP00000399685.1:n.*1154C>A | |
| ENST00000455843.5:c.*1154C>A (SEPTIN5) | ENSP00000391731.1:n.*1154C>A | |
| ENST00000470814.1:n.2041C>A (SEPTIN5) | ||
| NM_000407.4:c.69C>A , LRG_478t1:c.69C>A (GP1BB) | NP_000398.1:p.Ala23= | |
| NR_037611.1:n.3809C>A | ||
| NR_037612.1:n.2313C>A | ||
| NM_000407.5:c.69C>A (GP1BB) MANE Select | NP_000398.1:p.Ala23= |