HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215944_21215947delinsGGAT , CM000674.2:g.21215944_21215947delinsGGAT | GRCh38 |
NC_000012.11:g.21368878_21368881delinsGGAT , CM000674.1:g.21368878_21368881delinsGGAT | GRCh37 |
NC_000012.10:g.21260145_21260148delinsGGAT | NCBI36 |
NG_011745.1:g.89751_89754delinsGGAT , LRG_1022:g.89751_89754delinsGGAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1175_1498-1172delinsGGAT MANE Select | ENSP00000256958.2:n.1498-1175_1498-1172delinsGGAT | |
ENST00000256958.2:c.1498-1175_1498-1172delinsGGAT | ENSP00000256958.2:n.1498-1175_1498-1172delinsGGAT | |
NM_006446.4:c.1498-1175_1498-1172delinsGGAT , LRG_1022t1:c.1498-1175_1498-1172delinsGGAT | NP_006437.3:n.1498-1175_1498-1172delinsGGAT | |
NM_006446.5:c.1498-1175_1498-1172delinsGGAT MANE Select | NP_006437.3:n.1498-1175_1498-1172delinsGGAT |