HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94030662_94030669del , CM000663.2:g.94030662_94030669del | GRCh38 |
NC_000001.10:g.94496218_94496225del , CM000663.1:g.94496218_94496225del | GRCh37 |
NC_000001.9:g.94268806_94268813del | NCBI36 |
NG_009073.1:g.95482_95489del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4254-142_4254-135del MANE Select | ENSP00000359245.3:n.4254-142_4254-135del | |
ENST00000370225.3:c.4254-142_4254-135del | ENSP00000359245.3:n.4254-142_4254-135del | |
ENST00000536513.5:c.630-142_630-135del | ENSP00000439707.2:n.630-142_630-135del | |
NM_000350.2:c.4254-142_4254-135del | NP_000341.2:n.4254-142_4254-135del | |
NM_000350.3:c.4254-142_4254-135del MANE Select | NP_000341.2:n.4254-142_4254-135del |