HGVS | Genome Assembly |
---|---|
NC_000001.11:g.40784034dup , CM000663.2:g.40784034dup | GRCh38 |
NC_000001.10:g.41249706dup , CM000663.1:g.41249706dup | GRCh37 |
NC_000001.9:g.41022293dup | NCBI36 |
NG_008139.1:g.5023dup | |
NG_008139.2:g.5023dup | |
NG_008139.3:g.5248dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000347132.10:c.-60dup MANE Select | ENSP00000262916.6:n.-60dup | |
ENST00000347132.9:c.-60dup | ENSP00000262916.6:n.-60dup | |
NM_004700.3:c.-60dup | NP_004691.2:n.-60dup | |
NM_172163.2:c.-60dup | NP_751895.1:n.-60dup | |
NM_004700.4:c.-60dup MANE Select | NP_004691.2:n.-60dup | |
NM_172163.3:c.-60dup | NP_751895.1:n.-60dup |