HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6712908T= , CM000681.2:g.6712908T= | GRCh38 |
NC_000019.9:g.6712919T= , CM000681.1:g.6712919T= | GRCh37 |
NC_000019.8:g.6663919T= | NCBI36 |
NG_009557.1:g.12744A= , LRG_27:g.12744A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.880+281A= | ENSP00000512083.1:n.880+281A= | |
ENST00000695654.1:c.127+281A= | ENSP00000512085.1:n.127+281A= | |
ENST00000695692.1:n.328-245A= | ||
ENST00000245907.11:c.1003+281A= MANE Select | ENSP00000245907.4:n.1003+281A= | |
ENST00000245907.10:c.1003+281A= | ENSP00000245907.4:n.1003+281A= | |
ENST00000594270.5:n.127+281A= | ||
ENST00000595577.1:n.507+281A= | ||
ENST00000597442.5:n.253+281A= | ||
NM_000064.3:c.1003+281A= | NP_000055.2:n.1003+281A= | |
NM_000064.4:c.1003+281A= MANE Select | NP_000055.2:n.1003+281A= |