HGVS | Genome Assembly |
---|---|
NC_000001.11:g.168293291_168293297del , CM000663.2:g.168293291_168293297del | GRCh38 |
NC_000001.10:g.168262529_168262535del , CM000663.1:g.168262529_168262535del | GRCh37 |
NC_000001.9:g.166529153_166529159del | NCBI36 |
NG_008244.1:g.17252_17258del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367821.8:c.603+13_603+19del MANE Select | ENSP00000356795.3:n.603+13_603+19del | |
ENST00000367821.7:c.603+13_603+19del | ENSP00000356795.3:n.603+13_603+19del | |
ENST00000431969.5:c.400+13_400+19del | ||
NM_005149.2:c.603+13_603+19del | NP_005140.1:n.603+13_603+19del | |
NM_005149.3:c.603+13_603+19del MANE Select | NP_005140.1:n.603+13_603+19del |