HGVS | Genome Assembly |
---|---|
NC_000016.10:g.56609433G= , CM000678.2:g.56609433G= | GRCh38 |
NC_000016.9:g.56643345G= , CM000678.1:g.56643345G= | GRCh37 |
NC_000016.8:g.55200846G= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000245185.6:c.*79G= MANE Select | ENSP00000245185.5:n.*79G= | |
ENST00000245185.5:c.*79G= | ENSP00000245185.5:n.*79G= | |
ENST00000561491.1:c.*248G= | ENSP00000456804.1:n.*248G= | |
ENST00000562017.1:n.839G= | ||
ENST00000563985.1:n.645G= | ||
ENST00000567300.1:n.352G= | ||
NM_005953.3:c.*79G= | NP_005944.1:n.*79G= | |
XR_933616.1:n.1057C= | ||
NM_005953.4:c.*79G= | NP_005944.1:n.*79G= | |
NM_005953.5:c.*79G= MANE Select | NP_005944.1:n.*79G= |