HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10199716A= , CM000681.2:g.10199716A= | GRCh38 |
NC_000019.9:g.10310392A= , CM000681.1:g.10310392A= | GRCh37 |
NC_000019.8:g.10171392A= | NCBI36 |
NG_028016.3:g.36571T= , LRG_362:g.36571T= |
HGVS | Amino-acid Change |
---|---|
ENST00000586800.5:c.-284+1158T= | ENSP00000465555.1:n.-284+1158T= |
ENST00000588118.5:c.10+1158T= | ENSP00000465223.1:n.10+1158T= |
ENST00000588952.5:c.-283-17639T= | ENSP00000467050.1:n.-283-17639T= |
ENST00000592342.5:c.-283-17639T= | ENSP00000465993.1:n.-283-17639T= |