HGVS | Genome Assembly |
---|---|
NC_000016.10:g.56609333C= , CM000678.2:g.56609333C= | GRCh38 |
NC_000016.9:g.56643245C= , CM000678.1:g.56643245C= | GRCh37 |
NC_000016.8:g.55200746C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000245185.6:c.165C= MANE Select | ENSP00000245185.5:p.Asp55= | |
ENST00000245185.5:c.165C= | ENSP00000245185.5:p.Asp55= | |
ENST00000561491.1:c.*148C= | ENSP00000456804.1:n.*148C= | |
ENST00000562017.1:n.739C= | ||
ENST00000563985.1:n.545C= | ||
ENST00000567300.1:n.252C= | ||
NM_005953.3:c.165C= | NP_005944.1:p.Asp55= | |
NM_005953.4:c.165C= | NP_005944.1:p.Asp55= | |
NM_005953.5:c.165C= MANE Select | NP_005944.1:p.Asp55= |