HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19953970_19953974delinsGTCTC , CM000670.2:g.19953970_19953974delinsGTCTC | GRCh38 |
NC_000008.10:g.19811481_19811485delinsGTCTC , CM000670.1:g.19811481_19811485delinsGTCTC | GRCh37 |
NC_000008.9:g.19855761_19855765delinsGTCTC | NCBI36 |
NG_008855.1:g.19900_19904delinsGTCTC | |
NG_008855.2:g.57254_57258delinsGTCTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.542-150_542-146delinsGTCTC MANE Select | ENSP00000497642.1:n.542-150_542-146delinsGTCTC | |
ENST00000311322.8:c.542-150_542-146delinsGTCTC | ENSP00000309757.6:n.542-150_542-146delinsGTCTC | |
ENST00000520959.5:c.314-150_314-146delinsGTCTC | ENSP00000428496.1:n.314-150_314-146delinsGTCTC | |
NM_000237.2:c.542-150_542-146delinsGTCTC | NP_000228.1:n.542-150_542-146delinsGTCTC | |
NM_000237.3:c.542-150_542-146delinsGTCTC MANE Select | NP_000228.1:n.542-150_542-146delinsGTCTC |