HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1423708_1423710del , CM000667.2:g.1423708_1423710del | GRCh38 |
NC_000005.9:g.1423823_1423825del , CM000667.1:g.1423823_1423825del | GRCh37 |
NC_000005.8:g.1476823_1476825del | NCBI36 |
NG_015885.1:g.26721_26723del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.654-1694_654-1692del MANE Select | ENSP00000270349.9:n.654-1694_654-1692del | |
ENST00000270349.11:c.654-1694_654-1692del | ENSP00000270349.9:n.654-1694_654-1692del | |
NM_001044.4:c.654-1694_654-1692del | NP_001035.1:n.654-1694_654-1692del | |
NM_001044.5:c.654-1694_654-1692del MANE Select | NP_001035.1:n.654-1694_654-1692del |