HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101615902C= , CM000671.2:g.101615902C= | GRCh38 |
NC_000009.11:g.104378184C= , CM000671.1:g.104378184C= | GRCh37 |
NC_000009.10:g.103418005C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.2615-2375G= MANE Select | ENSP00000355155.3:n.2615-2375G= | |
ENST00000361820.3:c.2615-2375G= | ENSP00000355155.3:n.2615-2375G= | |
NM_133445.2:c.2615-2375G= | NP_597702.2:n.2615-2375G= | |
XM_011518211.1:c.2615-2375G= | XP_011516513.1:n.2615-2375G= | |
XM_011518212.1:c.2615-2375G= | XP_011516514.1:n.2615-2375G= | |
XR_929711.1:n.2702-2375G= | ||
XM_011518211.2:c.2615-2375G= | XP_011516513.1:n.2615-2375G= | |
NM_133445.3:c.2615-2375G= MANE Select | NP_597702.2:n.2615-2375G= |