HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160882150del , CM000663.2:g.160882150del | GRCh38 |
NC_000001.10:g.160851940del , CM000663.1:g.160851940del | GRCh37 |
NC_000001.9:g.159118564del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.212del MANE Select | ENSP00000323587.3:p.Asp71AlafsTer2 | |
ENST00000326245.3:c.212del | ENSP00000323587.3:p.Asp71AlafsTer2 | |
ENST00000464077.1:n.146del | ||
NM_017625.2:c.212del | NP_060095.2:p.Asp71AlafsTer2 | |
NM_017625.3:c.212del MANE Select | NP_060095.2:p.Asp71AlafsTer2 |