HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48875917T= , CM000681.2:g.48875917T= | GRCh38 |
NC_000019.9:g.49379174T= , CM000681.1:g.49379174T= | GRCh37 |
NC_000019.8:g.54070986T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000600406.2:c.*824T= | ENSP00000469239.2:n.*824T= | |
ENST00000704026.1:c.1684T= | ENSP00000515636.1:p.Ser562= | |
ENST00000704027.1:c.2017T= | ENSP00000515637.1:p.Ser673= | |
ENST00000200453.6:c.1969T= MANE Select | ENSP00000200453.4:p.Ser657= | |
ENST00000200453.5:c.1969T= | ENSP00000200453.4:p.Ser657= | |
ENST00000600406.1:c.1600T= | ||
NM_014330.3:c.1969T= | NP_055145.3:p.Ser657= | |
NM_014330.5:c.1969T= MANE Select | NP_055145.3:p.Ser657= |