HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48875812C= , CM000681.2:g.48875812C= | GRCh38 |
NC_000019.9:g.49379069C= , CM000681.1:g.49379069C= | GRCh37 |
NC_000019.8:g.54070881C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000600406.2:c.*719C= | ENSP00000469239.2:n.*719C= | |
ENST00000704026.1:c.1579C= | ENSP00000515636.1:p.Pro527= | |
ENST00000704027.1:c.1912C= | ENSP00000515637.1:p.Pro638= | |
ENST00000200453.6:c.1864C= MANE Select | ENSP00000200453.4:p.Pro622= | |
ENST00000200453.5:c.1864C= | ENSP00000200453.4:p.Pro622= | |
ENST00000600406.1:c.1495C= | ||
NM_014330.3:c.1864C= | NP_055145.3:p.Pro622= | |
NM_014330.5:c.1864C= MANE Select | NP_055145.3:p.Pro622= |