HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20992905del , CM000684.2:g.20992905del | GRCh38 |
NC_000022.10:g.21347194del , CM000684.1:g.21347194del | GRCh37 |
NC_000022.9:g.19677194del | NCBI36 |
NG_034193.1:g.15637del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000700578.1:c.1260+1del | ||
ENST00000495142.6:n.605+1del | ||
ENST00000642151.1:c.1091+1del | ||
ENST00000643578.1:n.1282+1del | ||
ENST00000646124.2:c.1260+1del | ||
ENST00000646506.1:n.839+1del | ||
ENST00000215739.12:c.1260+1del | ||
ENST00000479606.5:n.1406+1del | ||
ENST00000492480.1:n.309+8del | ||
NM_006767.3:c.1260+1del | ||
NM_006767.4:c.1260+1del |