HGVS | Genome Assembly |
---|---|
NC_000023.11:g.640796A= , CM000685.2:g.640796A= | GRCh38 |
NC_000023.10:g.601531A= , CM000685.1:g.601531A= | GRCh37 |
NC_000023.9:g.521531A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686671.1:c.487-25A= MANE Select | ENSP00000508521.1:n.487-25A= | |
ENST00000334060.8:c.487-25A= | ENSP00000335505.3:n.487-25A= | |
ENST00000381575.6:c.487-25A= | ENSP00000370987.1:n.487-25A= | |
ENST00000381578.6:c.487-25A= | ENSP00000370990.1:n.487-25A= | |
ENST00000554971.6:c.487-25A= | ENSP00000452016.1:n.487-25A= |