HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202666_32202668delinsACT , CM000668.2:g.32202666_32202668delinsACT | GRCh38 |
NC_000006.11:g.32170443_32170445delinsACT , CM000668.1:g.32170443_32170445delinsACT | GRCh37 |
NC_000006.10:g.32278421_32278423delinsACT | NCBI36 |
NG_028190.1:g.26400_26402delinsAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-69_3232-67delinsAGT MANE Select | ENSP00000364163.3:n.3232-69_3232-67delinsAGT | |
ENST00000474612.1:n.1249_1251delinsAGT | ||
NM_004557.3:c.3232-69_3232-67delinsAGT | NP_004548.3:n.3232-69_3232-67delinsAGT | |
NR_134949.1:n.3472+1102_3472+1104delinsAGT | ||
NR_134950.1:n.3370+1102_3370+1104delinsAGT | ||
NM_004557.4:c.3232-69_3232-67delinsAGT MANE Select | NP_004548.3:n.3232-69_3232-67delinsAGT | |
NR_134949.2:n.3472+1102_3472+1104delinsAGT | ||
NR_134950.2:n.3370+1102_3370+1104delinsAGT |