HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884887_13884889del , CM000680.2:g.13884887_13884889del | GRCh38 |
NC_000018.9:g.13884886_13884888del , CM000680.1:g.13884886_13884888del | GRCh37 |
NC_000018.8:g.13874886_13874888del | NCBI36 |
NG_011819.1:g.35649_35651del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.631_633del MANE Select | ENSP00000333821.2:p.Pro211del | |
ENST00000327606.3:c.631_633del | ENSP00000333821.2:p.Pro211del | |
NM_000529.2:c.631_633del MANE Select | NP_000520.1:p.Pro211del | |
NM_001291911.1:c.631_633del | NP_001278840.1:p.Pro211del | |
XM_017025781.1:c.631_633del | XP_016881270.1:p.Pro211del |