HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94007565_94007570del , CM000663.2:g.94007565_94007570del | GRCh38 |
NC_000001.10:g.94473121_94473126del , CM000663.1:g.94473121_94473126del | GRCh37 |
NC_000001.9:g.94245709_94245714del | NCBI36 |
NG_009073.1:g.118580_118585del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.6005+64_6005+69del MANE Select | ENSP00000359245.3:n.6005+64_6005+69del | |
ENST00000370225.3:c.6005+64_6005+69del | ENSP00000359245.3:n.6005+64_6005+69del | |
ENST00000465352.1:n.421+64_421+69del | ||
ENST00000484388.1:n.119+64_119+69del | ||
ENST00000536513.5:c.2381+64_2381+69del | ENSP00000439707.2:n.2381+64_2381+69del | |
NM_000350.2:c.6005+64_6005+69del | NP_000341.2:n.6005+64_6005+69del | |
NM_000350.3:c.6005+64_6005+69del MANE Select | NP_000341.2:n.6005+64_6005+69del |