HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19724319del , CM000684.2:g.19724319del | GRCh38 |
NC_000022.10:g.19711842del , CM000684.1:g.19711842del | GRCh37 |
NC_000022.9:g.18091842del | NCBI36 |
NG_007974.1:g.5777del , LRG_478:g.5777del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366425.4:c.476del (GP1BB) MANE Select | ENSP00000383382.2:p.Gly159AlafsTer? | |
ENST00000366425.3:c.476del (GP1BB) | ENSP00000383382.2:p.Gly159AlafsTer? | |
ENST00000431044.5:c.*1561del (SEPTIN5) | ENSP00000399685.1:n.*1561del | |
NM_000407.4:c.476del , LRG_478t1:c.476del (GP1BB) | NP_000398.1:p.Gly159AlafsTer? | |
NR_037611.1:n.4216del | ||
NR_037612.1:n.2720del | ||
NM_000407.5:c.476del (GP1BB) MANE Select | NP_000398.1:p.Gly159AlafsTer? |