HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131876985T= , CM000668.2:g.131876985T= | GRCh38 |
NC_000006.11:g.132198125T= , CM000668.1:g.132198125T= | GRCh37 |
NC_000006.10:g.132239818T= | NCBI36 |
NG_008206.1:g.73970T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000683687.1:n.596-7T= | ||
ENST00000684536.1:n.222-7T= | ||
ENST00000647893.1:c.1724-7T= MANE Select | ENSP00000498074.1:n.1724-7T= | |
ENST00000647981.1:n.409-7T= | ||
ENST00000650437.1:c.1215-7T= | ||
ENST00000360971.6:c.1724-7T= | ENSP00000354238.2:n.1724-7T= | |
ENST00000459624.1:n.768-7T= | ||
ENST00000513998.5:c.*561-7T= | ENSP00000422424.1:n.*561-7T= | |
NM_006208.2:c.1724-7T= | NP_006199.2:n.1724-7T= | |
XM_011535896.1:c.614-7T= | XP_011534198.1:n.614-7T= | |
NM_006208.3:c.1724-7T= MANE Select | NP_006199.2:n.1724-7T= |