HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640207_640214del , CM000673.2:g.640207_640214del | GRCh38 |
NC_000011.9:g.640207_640214del , CM000673.1:g.640207_640214del | GRCh37 |
NC_000011.8:g.630207_630214del | NCBI36 |
NG_021241.1:g.7903_7910del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000176183.6:c.958_965del MANE Select | ENSP00000176183.5:p.Ala320ThrfsTer? | |
ENST00000176183.5:c.958_965del | ENSP00000176183.5:p.Ala320ThrfsTer? | |
NM_000797.3:c.958_965del | NP_000788.2:p.Ala320ThrfsTer? | |
NM_000797.4:c.958_965del MANE Select | NP_000788.2:p.Ala320ThrfsTer? |