HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957637_19957638delinsGT , CM000670.2:g.19957637_19957638delinsGT | GRCh38 |
NC_000008.10:g.19815148_19815149delinsGT , CM000670.1:g.19815148_19815149delinsGT | GRCh37 |
NC_000008.9:g.19859428_19859429delinsGT | NCBI36 |
NG_008855.1:g.23567_23568delinsGT | |
NG_008855.2:g.60921_60922delinsGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1018+1554_1018+1555delinsGT MANE Select | ENSP00000497642.1:n.1018+1554_1018+1555de... | |
ENST00000650478.1:c.79+1554_79+1555delinsGT | ENSP00000497560.1:n.79+1554_79+1555delins... | |
ENST00000311322.8:c.1018+1554_1018+1555delinsGT | ENSP00000309757.6:n.1018+1554_1018+1555de... | |
NM_000237.2:c.1018+1554_1018+1555delinsGT | NP_000228.1:n.1018+1554_1018+1555delinsGT... | |
NM_000237.3:c.1018+1554_1018+1555delinsGT MANE Select | NP_000228.1:n.1018+1554_1018+1555delinsGT... |