HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202655_32202656insT , CM000668.2:g.32202655_32202656insT | GRCh38 |
NC_000006.11:g.32170432_32170433insT , CM000668.1:g.32170432_32170433insT | GRCh37 |
NC_000006.10:g.32278410_32278411insT | NCBI36 |
NG_028190.1:g.26412_26413insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-57_3232-56insA MANE Select | ENSP00000364163.3:n.3232-57_3232-56insA | |
ENST00000474612.1:n.1261_1262insA | ||
NM_004557.3:c.3232-57_3232-56insA | NP_004548.3:n.3232-57_3232-56insA | |
NR_134949.1:n.3472+1114_3472+1115insA | ||
NR_134950.1:n.3370+1114_3370+1115insA | ||
NM_004557.4:c.3232-57_3232-56insA MANE Select | NP_004548.3:n.3232-57_3232-56insA | |
NR_134949.2:n.3472+1114_3472+1115insA | ||
NR_134950.2:n.3370+1114_3370+1115insA |