HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22624992del , CM000673.2:g.22624992del | GRCh38 |
NC_000011.9:g.22646538del , CM000673.1:g.22646538del | GRCh37 |
NC_000011.8:g.22603114del | NCBI36 |
NG_007425.1:g.5850del , LRG_527:g.5850del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.819del MANE Select | ENSP00000330875.3:p.Tyr274IlefsTer5 | |
ENST00000327470.4:c.819del | ENSP00000330875.3:p.Tyr274IlefsTer5 | |
NM_022725.3:c.819del , LRG_527t1:c.819del | NP_073562.1:p.Tyr274IlefsTer5 | |
NM_022725.4:c.819del MANE Select | NP_073562.1:p.Tyr274IlefsTer5 |