HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6712947A= , CM000681.2:g.6712947A= | GRCh38 |
NC_000019.9:g.6712958A= , CM000681.1:g.6712958A= | GRCh37 |
NC_000019.8:g.6663958A= | NCBI36 |
NG_009557.1:g.12705T= , LRG_27:g.12705T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.880+242T= | ENSP00000512083.1:n.880+242T= | |
ENST00000695654.1:c.127+242T= | ENSP00000512085.1:n.127+242T= | |
ENST00000695692.1:n.327+242T= | ||
ENST00000245907.11:c.1003+242T= MANE Select | ENSP00000245907.4:n.1003+242T= | |
ENST00000245907.10:c.1003+242T= | ENSP00000245907.4:n.1003+242T= | |
ENST00000594270.5:n.127+242T= | ||
ENST00000595577.1:n.507+242T= | ||
ENST00000597442.5:n.253+242T= | ||
NM_000064.3:c.1003+242T= | NP_000055.2:n.1003+242T= | |
NM_000064.4:c.1003+242T= MANE Select | NP_000055.2:n.1003+242T= |