HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202898_32202899insAA , CM000668.2:g.32202898_32202899insAA | GRCh38 |
NC_000006.11:g.32170675_32170676insAA , CM000668.1:g.32170675_32170676insAA | GRCh37 |
NC_000006.10:g.32278653_32278654insAA | NCBI36 |
NG_028190.1:g.26169_26170insTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-300_3232-299insTT MANE Select | ENSP00000364163.3:n.3232-300_3232-299insTT | |
ENST00000474612.1:n.1018_1019insTT | ||
NM_004557.3:c.3232-300_3232-299insTT | NP_004548.3:n.3232-300_3232-299insTT | |
NR_134949.1:n.3472+871_3472+872insTT | ||
NR_134950.1:n.3370+871_3370+872insTT | ||
NM_004557.4:c.3232-300_3232-299insTT MANE Select | NP_004548.3:n.3232-300_3232-299insTT | |
NR_134949.2:n.3472+871_3472+872insTT | ||
NR_134950.2:n.3370+871_3370+872insTT |