HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6709798A= , CM000681.2:g.6709798A= | GRCh38 |
NC_000019.9:g.6709809A= , CM000681.1:g.6709809A= | GRCh37 |
NC_000019.8:g.6660809A= | NCBI36 |
NG_009557.1:g.15854T= , LRG_27:g.15854T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.1608T= | ENSP00000512083.1:p.Pro536= | |
ENST00000695654.1:c.855T= | ENSP00000512085.1:p.Pro285= | |
ENST00000695655.1:c.672T= | ENSP00000512086.1:n.672T= | |
ENST00000695692.1:n.1095T= | ||
ENST00000245907.11:c.1731T= MANE Select | ENSP00000245907.4:p.Pro577= | |
ENST00000245907.10:c.1731T= | ENSP00000245907.4:p.Pro577= | |
ENST00000600763.1:n.364T= | ||
NM_000064.3:c.1731T= | NP_000055.2:p.Pro577= | |
NM_000064.4:c.1731T= MANE Select | NP_000055.2:p.Pro577= |