HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21178624del , CM000674.2:g.21178624del | GRCh38 |
NC_000012.11:g.21331558del , CM000674.1:g.21331558del | GRCh37 |
NC_000012.10:g.21222825del | NCBI36 |
NG_011745.1:g.52431del , LRG_1022:g.52431del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.530del MANE Select | ENSP00000256958.2:p.Gly177ValfsTer7 | |
ENST00000256958.2:c.530del | ENSP00000256958.2:p.Gly177ValfsTer7 | |
NM_006446.4:c.530del , LRG_1022t1:c.530del | NP_006437.3:p.Gly177ValfsTer7 | |
NM_006446.5:c.530del MANE Select | NP_006437.3:p.Gly177ValfsTer7 |