HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35284903_35284906del , CM000681.2:g.35284903_35284906del | GRCh38 |
NC_000019.9:g.35775806_35775809del , CM000681.1:g.35775806_35775809del | GRCh37 |
NC_000019.8:g.40467646_40467649del | NCBI36 |
NG_011563.1:g.7397_7400del | |
NG_011563.2:g.7397_7400del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000222304.5:c.151-35_151-32del MANE Select | ENSP00000222304.2:n.151-35_151-32del | |
ENST00000222304.3:c.151-35_151-32del | ENSP00000222304.2:n.151-35_151-32del | |
ENST00000593580.1:n.2387_2390del | ||
ENST00000598398.5:c.151-35_151-32del | ENSP00000471894.1:n.151-35_151-32del | |
NM_021175.2:c.151-35_151-32del | NP_066998.1:n.151-35_151-32del | |
NM_021175.3:c.151-35_151-32del | NP_066998.1:n.151-35_151-32del | |
NM_021175.4:c.151-35_151-32del MANE Select | NP_066998.1:n.151-35_151-32del |