HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47733756del , CM000679.2:g.47733756del | GRCh38 |
NC_000017.10:g.45811122del , CM000679.1:g.45811122del | GRCh37 |
NC_000017.9:g.43166121del | NCBI36 |
NG_012166.1:g.5513del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000177694.2:c.302del MANE Select | ENSP00000177694.1:p.Gly101AlafsTer? | |
ENST00000177694.1:c.302del | ENSP00000177694.1:p.Gly101AlafsTer? | |
ENST00000581328.1:n.332del | ||
NM_013351.1:c.302del | NP_037483.1:p.Gly101AlafsTer? | |
XM_011524698.1:c.302del | XP_011523000.1:p.Gly101AlafsTer? | |
NM_013351.2:c.302del MANE Select | NP_037483.1:p.Gly101AlafsTer? |