HGVS | Genome Assembly |
---|---|
NC_000001.11:g.168293041_168293044delinsGGGT , CM000663.2:g.168293041_168293044delinsGGGT | GRCh38 |
NC_000001.10:g.168262279_168262282delinsGGGT , CM000663.1:g.168262279_168262282delinsGGGT | GRCh37 |
NC_000001.9:g.166528903_166528906delinsGGGT | NCBI36 |
NG_008244.1:g.17002_17005delinsGGGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367821.8:c.469-103_469-100delinsGGGT MANE Select | ENSP00000356795.3:n.469-103_469-100delinsGGGT | |
ENST00000367821.7:c.469-103_469-100delinsGGGT | ENSP00000356795.3:n.469-103_469-100delinsGGGT | |
ENST00000431969.5:c.266-103_266-100delinsGGGT | ||
NM_005149.2:c.469-103_469-100delinsGGGT | NP_005140.1:n.469-103_469-100delinsGGGT | |
NM_005149.3:c.469-103_469-100delinsGGGT MANE Select | NP_005140.1:n.469-103_469-100delinsGGGT |