HGVS | Genome Assembly |
---|---|
NC_000001.11:g.247896410_247896411delinsCA , CM000663.2:g.247896410_247896411delinsCA | GRCh38 |
NC_000001.10:g.248059712_248059713delinsCA , CM000663.1:g.248059712_248059713delinsCA | GRCh37 |
NC_000001.9:g.246126335_246126336delinsCA | NCBI36 |
NG_053132.1:g.5824_5825delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360358.3:c.824_825delinsCA MANE Select | ENSP00000353516.3:p.Met275Thr | |
NM_001001957.2:c.824_825delinsCA MANE Select | NP_001001957.2:p.Met275Thr |