HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48875910C>T , CM000681.2:g.48875910C>T | GRCh38 |
NC_000019.9:g.49379167C>T , CM000681.1:g.49379167C>T | GRCh37 |
NC_000019.8:g.54070979C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000600406.2:c.*817C>T | ENSP00000469239.2:n.*817C>T | |
ENST00000704026.1:c.1677C>T | ENSP00000515636.1:p.Ala559= | |
ENST00000704027.1:c.2010C>T | ENSP00000515637.1:p.Ala670= | |
ENST00000200453.6:c.1962C>T MANE Select | ENSP00000200453.4:p.Ala654= | |
ENST00000200453.5:c.1962C>T | ENSP00000200453.4:p.Ala654= | |
ENST00000600406.1:c.1593C>T | ||
NM_014330.3:c.1962C>T | NP_055145.3:p.Ala654= | |
NM_014330.5:c.1962C>T MANE Select | NP_055145.3:p.Ala654= |