HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101615830A= , CM000671.2:g.101615830A= | GRCh38 |
NC_000009.11:g.104378112A= , CM000671.1:g.104378112A= | GRCh37 |
NC_000009.10:g.103417933A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.2615-2303T= MANE Select | ENSP00000355155.3:n.2615-2303T= | |
ENST00000361820.3:c.2615-2303T= | ENSP00000355155.3:n.2615-2303T= | |
NM_133445.2:c.2615-2303T= | NP_597702.2:n.2615-2303T= | |
XM_011518211.1:c.2615-2303T= | XP_011516513.1:n.2615-2303T= | |
XM_011518212.1:c.2615-2303T= | XP_011516514.1:n.2615-2303T= | |
XR_929711.1:n.2702-2303T= | ||
XM_011518211.2:c.2615-2303T= | XP_011516513.1:n.2615-2303T= | |
NM_133445.3:c.2615-2303T= MANE Select | NP_597702.2:n.2615-2303T= |