HGVS | Genome Assembly |
---|---|
NC_000009.12:g.93953766_93953776delinsGCAGATGTTTC , CM000671.2:g.93953766_93953776delinsGCAGATGTTTC | GRCh38 |
NC_000009.11:g.96716048_96716058delinsGCAGATGTTTC , CM000671.1:g.96716048_96716058delinsGCAGATGTTTC | GRCh37 |
NC_000009.10:g.95755869_95755879delinsGCAGATGTTTC | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000253968.11:c.224-589_224-579delinsGAAACATCTGC MANE Select | ENSP00000253968.5:n.224-589_224-579delinsGAAACATCTGC | |
ENST00000253968.10:c.224-589_224-579delinsGAAACATCTGC | ENSP00000253968.5:n.224-589_224-579delinsGAAACATCTGC | |
NM_021570.3:c.224-589_224-579delinsGAAACATCTGC | NP_067545.3:n.224-589_224-579delinsGAAACATCTGC | |
NM_021570.4:c.224-589_224-579delinsGAAACATCTGC MANE Select | NP_067545.3:n.224-589_224-579delinsGAAACATCTGC |