HGVS | Genome Assembly |
---|---|
NC_000012.12:g.51913351del , CM000674.2:g.51913351del | GRCh38 |
NC_000012.11:g.52307135del , CM000674.1:g.52307135del | GRCh37 |
NC_000012.10:g.50593402del | NCBI36 |
NG_009549.1:g.10934del , LRG_543:g.10934del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000547400.6:c.355+1del | ||
ENST00000551576.6:c.313+1del | ||
ENST00000552678.2:c.313+1del | ||
ENST00000388922.9:c.313+1del | ||
ENST00000388922.8:c.313+1del | ||
ENST00000419526.6:c.103+816del | ENSP00000392492.2:n.103+816del | |
ENST00000547400.5:c.355+1del | ||
ENST00000550683.5:c.355+1del | ||
NM_000020.2:c.313+1del , LRG_543t1:c.313+1del | ||
NM_001077401.1:c.313+1del | ||
XM_005269235.2:c.313+1del | ||
XM_011539008.1:c.355+1del | ||
XM_024449279.1:c.-377+1del | ||
NM_000020.3:c.313+1del | ||
NM_001077401.2:c.313+1del |