HGVS | Genome Assembly |
---|---|
NC_000023.11:g.29622579T= , CM000685.2:g.29622579T= | GRCh38 |
NC_000023.10:g.29640696T= , CM000685.1:g.29640696T= | GRCh37 |
NC_000023.9:g.29550617T= | NCBI36 |
NG_008292.1:g.1040016T= | |
NG_008292.2:g.1040016T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378993.6:c.704-45851T= MANE Select | ENSP00000368278.1:n.704-45851T= | |
ENST00000378993.5:c.704-45851T= | ENSP00000368278.1:n.704-45851T= | |
NM_014271.3:c.704-45851T= | NP_055086.1:n.704-45851T= | |
XM_005274441.1:c.704-45851T= | XP_005274498.1:n.704-45851T= | |
XM_011545445.1:c.704-45851T= | XP_011543747.1:n.704-45851T= | |
XM_017029240.1:c.704-45851T= | XP_016884729.1:n.704-45851T= | |
XM_017029241.1:c.326-45851T= | XP_016884730.1:n.326-45851T= | |
NM_014271.4:c.704-45851T= MANE Select | NP_055086.1:n.704-45851T= |