HGVS | Genome Assembly |
---|---|
NC_000003.12:g.93896576del , CM000665.2:g.93896576del | GRCh38 |
NC_000003.11:g.93615420del , CM000665.1:g.93615420del | GRCh37 |
NC_000003.10:g.95098110del | NCBI36 |
NG_009813.1:g.82516del , LRG_572:g.82516del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000348974.5:c.965+1del | ||
ENST00000394236.9:c.965+1del | ||
ENST00000407433.6:c.920+1del | ||
ENST00000647936.1:c.965+1del | ||
ENST00000648381.1:n.1133+1del | ||
ENST00000648853.1:c.923+1del | ||
ENST00000649103.1:c.1064+1del | ||
ENST00000650591.1:c.1061+1del | ||
ENST00000394236.7:c.965+1del | ||
ENST00000407433.5:c.572+1del | ||
NM_000313.3:c.965+1del , LRG_572t1:c.965+1del | ||
NM_001314077.1:c.1061+1del , LRG_572t2:c.1061+1del | ||
NM_000313.4:c.965+1del | ||
NM_001314077.2:c.1061+1del |