HGVS | Genome Assembly |
---|---|
NC_000015.10:g.40932019A= , CM000677.2:g.40932019A= | GRCh38 |
NC_000015.9:g.41224217A= , CM000677.1:g.41224217A= | GRCh37 |
NC_000015.8:g.39011509A= | NCBI36 |
NG_046974.1:g.7687A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000249749.7:c.659-152A= MANE Select | ENSP00000249749.5:n.659-152A= | |
ENST00000249749.6:c.659-152A= | ENSP00000249749.5:n.659-152A= | |
ENST00000559440.1:n.888-152A= | ||
NM_019074.3:c.659-152A= | NP_061947.1:n.659-152A= | |
NM_019074.4:c.659-152A= MANE Select | NP_061947.1:n.659-152A= |