HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884932_13884933del , CM000680.2:g.13884932_13884933del | GRCh38 |
NC_000018.9:g.13884931_13884932del , CM000680.1:g.13884931_13884932del | GRCh37 |
NC_000018.8:g.13874931_13874932del | NCBI36 |
NG_011819.1:g.35604_35605del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.586_587del MANE Select | ENSP00000333821.2:p.Met196ValfsTer? | |
ENST00000327606.3:c.586_587del | ENSP00000333821.2:p.Met196ValfsTer? | |
NM_000529.2:c.586_587del MANE Select | NP_000520.1:p.Met196ValfsTer? | |
NM_001291911.1:c.586_587del | NP_001278840.1:p.Met196ValfsTer? | |
XM_017025781.1:c.586_587del | XP_016881270.1:p.Met196ValfsTer? |