HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150948445del , CM000669.2:g.150948445del | GRCh38 |
NC_000007.13:g.150645533del , CM000669.1:g.150645533del | GRCh37 |
NC_000007.12:g.150276466del | NCBI36 |
NG_008916.1:g.34484del , LRG_288:g.34484del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000684241.1:n.3525+1del | ||
ENST00000262186.10:c.2692+1del | ||
ENST00000330883.9:c.1672+1del | ||
ENST00000262186.9:c.2692+1del | ||
ENST00000330883.8:c.1672+1del | ||
NM_000238.3:c.2692+1del , LRG_288t1:c.2692+1del | ||
NM_172057.2:c.1672+1del , LRG_288t3:c.1672+1del | ||
XM_011516185.1:c.2392+1del | ||
XM_011516186.1:c.2692+1del | ||
XM_011516185.2:c.2392+1del | ||
XM_011516186.3:c.2692+1del | ||
XM_017012195.1:c.2542+1del | ||
XM_017012196.1:c.2515+1del | ||
NM_000238.4:c.2692+1del | ||
NM_172057.3:c.1672+1del |