HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94015686_94015691del , CM000663.2:g.94015686_94015691del | GRCh38 |
NC_000001.10:g.94481242_94481247del , CM000663.1:g.94481242_94481247del | GRCh37 |
NC_000001.9:g.94253830_94253835del | NCBI36 |
NG_009073.1:g.110467_110472del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.5312+56_5312+61del MANE Select | ENSP00000359245.3:n.5312+56_5312+61del | |
ENST00000370225.3:c.5312+56_5312+61del | ENSP00000359245.3:n.5312+56_5312+61del | |
ENST00000536513.5:c.1688+56_1688+61del | ENSP00000439707.2:n.1688+56_1688+61del | |
NM_000350.2:c.5312+56_5312+61del | NP_000341.2:n.5312+56_5312+61del | |
NM_000350.3:c.5312+56_5312+61del MANE Select | NP_000341.2:n.5312+56_5312+61del |