HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12695451_12695452del , CM000671.2:g.12695451_12695452del | GRCh38 |
NC_000009.11:g.12695451_12695452del , CM000671.1:g.12695451_12695452del | GRCh37 |
NC_000009.10:g.12685451_12685452del | NCBI36 |
NG_011705.1:g.7066_7067del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000388918.10:c.386-64_386-63del MANE Select | ENSP00000373570.4:n.386-64_386-63del | |
ENST00000388918.9:c.386-64_386-63del | ENSP00000373570.4:n.386-64_386-63del | |
NM_000550.2:c.386-64_386-63del | NP_000541.1:n.386-64_386-63del | |
XR_001746372.2:n.575-64_575-63del | ||
NM_000550.3:c.386-64_386-63del MANE Select | NP_000541.1:n.386-64_386-63del |