HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94002101del , CM000663.2:g.94002101del | GRCh38 |
NC_000001.10:g.94467657del , CM000663.1:g.94467657del | GRCh37 |
NC_000001.9:g.94240245del | NCBI36 |
NG_009073.1:g.124052del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.6148-106del MANE Select | ENSP00000359245.3:n.6148-106del | |
ENST00000370225.3:c.6148-106del | ENSP00000359245.3:n.6148-106del | |
ENST00000465352.1:n.564-106del | ||
ENST00000536513.5:c.2524-106del | ENSP00000439707.2:n.2524-106del | |
NM_000350.2:c.6148-106del | NP_000341.2:n.6148-106del | |
NM_000350.3:c.6148-106del MANE Select | NP_000341.2:n.6148-106del |