HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94853065_94853066del , CM000672.2:g.94853065_94853066del | GRCh38 |
NC_000010.10:g.96612822_96612823del , CM000672.1:g.96612822_96612823del | GRCh37 |
NC_000010.9:g.96602812_96602813del | NCBI36 |
NG_008384.2:g.95360_95361del | |
NG_008384.3:g.95385_95386del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.*151_*152del MANE Select | ENSP00000360372.3:n.*151_*152del | |
ENST00000645461.1:n.2535_2536del | ||
ENST00000371321.7:c.*151_*152del | ENSP00000360372.3:n.*151_*152del | |
ENST00000464755.1:c.2387_2388del | ENSP00000483243.1:n.2387_2388del | |
NM_000769.2:c.*151_*152del | NP_000760.1:n.*151_*152del | |
NM_000769.4:c.*151_*152del MANE Select | NP_000760.1:n.*151_*152del |