HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94056841_94056843del , CM000663.2:g.94056841_94056843del | GRCh38 |
NC_000001.10:g.94522397_94522399del , CM000663.1:g.94522397_94522399del | GRCh37 |
NC_000001.9:g.94294985_94294987del | NCBI36 |
NG_009073.1:g.69307_69309del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2161-21_2161-19del MANE Select | ENSP00000359245.3:n.2161-21_2161-19del | |
ENST00000649773.1:c.2161-1528_2161-1526del | ENSP00000496882.1:n.2161-1528_2161-1526del | |
ENST00000370225.3:c.2161-21_2161-19del | ENSP00000359245.3:n.2161-21_2161-19del | |
ENST00000536513.5:c.-65+6331_-65+6333del | ENSP00000439707.2:n.-65+6331_-65+6333del | |
NM_000350.2:c.2161-21_2161-19del | NP_000341.2:n.2161-21_2161-19del | |
NM_000350.3:c.2161-21_2161-19del MANE Select | NP_000341.2:n.2161-21_2161-19del |