HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013668_25013691del , CM000685.2:g.25013668_25013691del | GRCh38 |
NC_000023.10:g.25031785_25031808del , CM000685.1:g.25031785_25031808del | GRCh37 |
NC_000023.9:g.24941706_24941729del | NCBI36 |
NG_008281.1:g.7266_7289del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.312_335del MANE Select | ENSP00000368332.4:p.Ala105_Ala112del | |
ENST00000379044.4:c.312_335del | ENSP00000368332.4:p.Ala105_Ala112del | |
NM_139058.2:c.312_335del | NP_620689.1:p.Ala105_Ala112del | |
NM_139058.3:c.312_335del MANE Select | NP_620689.1:p.Ala105_Ala112del |