HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94056840_94056842del , CM000663.2:g.94056840_94056842del | GRCh38 |
NC_000001.10:g.94522396_94522398del , CM000663.1:g.94522396_94522398del | GRCh37 |
NC_000001.9:g.94294984_94294986del | NCBI36 |
NG_009073.1:g.69308_69310del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2161-20_2161-18del MANE Select | ENSP00000359245.3:n.2161-20_2161-18del | |
ENST00000649773.1:c.2161-1527_2161-1525del | ENSP00000496882.1:n.2161-1527_2161-1525del | |
ENST00000370225.3:c.2161-20_2161-18del | ENSP00000359245.3:n.2161-20_2161-18del | |
ENST00000536513.5:c.-65+6332_-65+6334del | ENSP00000439707.2:n.-65+6332_-65+6334del | |
NM_000350.2:c.2161-20_2161-18del | NP_000341.2:n.2161-20_2161-18del | |
NM_000350.3:c.2161-20_2161-18del MANE Select | NP_000341.2:n.2161-20_2161-18del |