HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101615650del , CM000671.2:g.101615650del | GRCh38 |
NC_000009.11:g.104377932del , CM000671.1:g.104377932del | GRCh37 |
NC_000009.10:g.103417753del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.2615-2121del MANE Select | ENSP00000355155.3:n.2615-2121del | |
ENST00000361820.3:c.2615-2121del | ENSP00000355155.3:n.2615-2121del | |
NM_133445.2:c.2615-2121del | NP_597702.2:n.2615-2121del | |
XM_011518211.1:c.2615-2121del | XP_011516513.1:n.2615-2121del | |
XM_011518212.1:c.2615-2121del | XP_011516514.1:n.2615-2121del | |
XR_929711.1:n.2702-2121del | ||
XM_011518211.2:c.2615-2121del | XP_011516513.1:n.2615-2121del | |
NM_133445.3:c.2615-2121del MANE Select | NP_597702.2:n.2615-2121del |