HGVS | Genome Assembly |
---|---|
NC_000009.12:g.93953333_93953345del , CM000671.2:g.93953333_93953345del | GRCh38 |
NC_000009.11:g.96715615_96715627del , CM000671.1:g.96715615_96715627del | GRCh37 |
NC_000009.10:g.95755436_95755448del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253968.11:c.224-158_224-146del MANE Select | ENSP00000253968.5:n.224-158_224-146del | |
ENST00000253968.10:c.224-158_224-146del | ENSP00000253968.5:n.224-158_224-146del | |
ENST00000401724.1:c.-397_-385del | ENSP00000385613.1:n.-397_-385del | |
NM_021570.3:c.224-158_224-146del | NP_067545.3:n.224-158_224-146del | |
NM_021570.4:c.224-158_224-146del MANE Select | NP_067545.3:n.224-158_224-146del |