HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94043512_94043517dup , CM000663.2:g.94043512_94043517dup | GRCh38 |
NC_000001.10:g.94509068_94509073dup , CM000663.1:g.94509068_94509073dup | GRCh37 |
NC_000001.9:g.94281656_94281661dup | NCBI36 |
NG_009073.1:g.82633_82638dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.3051-42_3051-37dup MANE Select | ENSP00000359245.3:n.3051-42_3051-37dup | |
ENST00000370225.3:c.3051-42_3051-37dup | ENSP00000359245.3:n.3051-42_3051-37dup | |
ENST00000536513.5:c.-64-3428_-64-3423dup | ENSP00000439707.2:n.-64-3428_-64-3423dup | |
NM_000350.2:c.3051-42_3051-37dup | NP_000341.2:n.3051-42_3051-37dup | |
NM_000350.3:c.3051-42_3051-37dup MANE Select | NP_000341.2:n.3051-42_3051-37dup |