HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202900_32202903delinsATAT , CM000668.2:g.32202900_32202903delinsATAT | GRCh38 |
NC_000006.11:g.32170677_32170680delinsATAT , CM000668.1:g.32170677_32170680delinsATAT | GRCh37 |
NC_000006.10:g.32278655_32278658delinsATAT | NCBI36 |
NG_028190.1:g.26165_26168delinsATAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-304_3232-301delinsATAT MANE Select | ENSP00000364163.3:n.3232-304_3232-301delinsATAT | |
ENST00000474612.1:n.1014_1017delinsATAT | ||
NM_004557.3:c.3232-304_3232-301delinsATAT | NP_004548.3:n.3232-304_3232-301delinsATAT | |
NR_134949.1:n.3472+867_3472+870delinsATAT | ||
NR_134950.1:n.3370+867_3370+870delinsATAT | ||
NM_004557.4:c.3232-304_3232-301delinsATAT MANE Select | NP_004548.3:n.3232-304_3232-301delinsATAT | |
NR_134949.2:n.3472+867_3472+870delinsATAT | ||
NR_134950.2:n.3370+867_3370+870delinsATAT |