HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48441721del , CM000677.2:g.48441721del | GRCh38 |
NC_000015.9:g.48733918del , CM000677.1:g.48733918del | GRCh37 |
NC_000015.8:g.46521210del | NCBI36 |
NG_008805.2:g.209069del , LRG_778:g.209069del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000559133.6:c.6163+1del | ||
ENST00000674301.2:c.6163+1del | ||
ENST00000316623.10:c.6163+1del | ||
ENST00000674301.1:c.1162+1del | ||
ENST00000316623.9:c.6163+1del | ||
ENST00000537463.6:c.*1926+1del | ||
ENST00000559133.5:c.1470+1del | ||
ENST00000560820.1:n.283+1del | ||
NM_000138.4:c.6163+1del , LRG_778t1:c.6163+1del | ||
NM_000138.5:c.6163+1del |