HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32043267_32043268insT , CM000684.2:g.32043267_32043268insT | GRCh38 |
NC_000022.10:g.32439254_32439255insT , CM000684.1:g.32439254_32439255insT | GRCh37 |
NC_000022.9:g.30769254_30769255insT | NCBI36 |
NG_017045.1:g.5236_5237insT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266088.9:c.-15_-14insT MANE Select | ENSP00000266088.4:n.-15_-14insT | |
ENST00000266088.8:c.-15_-14insT | ENSP00000266088.4:n.-15_-14insT | |
NM_000343.3:c.-15_-14insT | NP_000334.1:n.-15_-14insT | |
XM_011530331.1:c.-15_-14insT | XP_011528633.1:n.-15_-14insT | |
NM_000343.4:c.-15_-14insT MANE Select | NP_000334.1:n.-15_-14insT |