HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67942836C= , CM000678.2:g.67942836C= | GRCh38 |
NC_000016.9:g.67976739C= , CM000678.1:g.67976739C= | GRCh37 |
NC_000016.8:g.66534240C= | NCBI36 |
NG_009778.1:g.6277G= | |
NG_033098.1:g.30859G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264005.10:c.427+25G= MANE Select | ENSP00000264005.5:n.427+25G= | |
ENST00000264005.9:c.427+25G= | ENSP00000264005.5:n.427+25G= | |
ENST00000570369.5:c.155+25G= | ||
ENST00000570980.1:c.211+25G= | ENSP00000464651.1:n.211+25G= | |
ENST00000573538.5:c.70+25G= | ENSP00000463220.1:n.70+25G= | |
ENST00000573846.1:n.41+25G= | ||
ENST00000575277.1:n.205+25G= | ||
ENST00000575467.5:c.*122+25G= | ENSP00000460653.1:n.*122+25G= | |
NM_000229.1:c.427+25G= | NP_000220.1:n.427+25G= | |
NM_000229.2:c.427+25G= MANE Select | NP_000220.1:n.427+25G= |