HGVS | Genome Assembly |
---|---|
NC_000019.10:g.17830219del , CM000681.2:g.17830219del | GRCh38 |
NC_000019.9:g.17941028del , CM000681.1:g.17941028del | GRCh37 |
NC_000019.8:g.17802028del | NCBI36 |
NG_007273.1:g.22774del , LRG_77:g.22774del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000526008.6:c.*1654del | ||
ENST00000696967.1:n.2274del | ||
ENST00000696968.1:n.330del | ||
ENST00000696969.1:n.2054del | ||
ENST00000458235.7:c.3097del | ||
ENST00000458235.5:c.3097del | ||
ENST00000527031.5:n.2279-4908del | ||
ENST00000527670.5:c.3097del | ||
ENST00000534444.1:c.3097del | ||
NM_000215.3:c.3097del , LRG_77t1:c.3097del | ||
XM_005259896.2:c.3226del | ||
XM_006722745.2:c.3097del | ||
XM_005259896.3:c.3226del | ||
NM_000215.4:c.3097del |