HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4932854_4932862del , CM000679.2:g.4932854_4932862del | GRCh38 |
NC_000017.10:g.4836149_4836157del , CM000679.1:g.4836149_4836157del | GRCh37 |
NC_000017.9:g.4776929_4776937del | NCBI36 |
NG_008767.2:g.5560_5568del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329125.6:c.250_258del (GP1BA) MANE Select | ENSP00000329380.5:p.Thr84_Leu86del | |
ENST00000649830.1:c.-888+1485_-888+1493del (CHRNE) | ENSP00000496907.1:n.-888+1485_-888+1493del | |
ENST00000329125.5:c.250_258del (GP1BA) | ENSP00000329380.5:p.Thr84_Leu86del | |
ENST00000611961.1:c.250_258del (GP1BA) | ENSP00000484439.1:p.Thr84_Leu86del | |
NM_000173.6:c.250_258del (GP1BA) | NP_000164.5:p.Thr84_Leu86del | |
NM_000173.7:c.250_258del (GP1BA) MANE Select | NP_000164.5:p.Thr84_Leu86del |