HGVS | Genome Assembly |
---|---|
NC_000001.11:g.40784062del , CM000663.2:g.40784062del | GRCh38 |
NC_000001.10:g.41249734del , CM000663.1:g.41249734del | GRCh37 |
NC_000001.9:g.41022321del | NCBI36 |
NG_008139.1:g.5051del | |
NG_008139.2:g.5051del | |
NG_008139.3:g.5276del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000347132.10:c.-32del MANE Select | ENSP00000262916.6:n.-32del | |
ENST00000347132.9:c.-32del | ENSP00000262916.6:n.-32del | |
NM_004700.3:c.-32del | NP_004691.2:n.-32del | |
NM_172163.2:c.-32del | NP_751895.1:n.-32del | |
NM_004700.4:c.-32del MANE Select | NP_004691.2:n.-32del | |
NM_172163.3:c.-32del | NP_751895.1:n.-32del |