HGVS | Genome Assembly |
---|---|
NC_000007.14:g.151187300_151187301del , CM000669.2:g.151187300_151187301del | GRCh38 |
NC_000007.13:g.150884387_150884388del , CM000669.1:g.150884387_150884388del | GRCh37 |
NC_000007.12:g.150515320_150515321del | NCBI36 |
NG_017016.1:g.5535_5536del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000275838.5:c.-168_-167del | ENSP00000275838.1:n.-168_-167del | |
ENST00000377867.7:c.271+154_271+155del | ENSP00000367098.3:n.271+154_271+155del | |
ENST00000415615.1:c.*77_*78del | ENSP00000410871.1:n.*77_*78del | |
NM_001142459.1:c.-168_-167del | NP_001135931.2:n.-168_-167del | |
NM_001142460.1:c.-168_-167del | NP_001135932.2:n.-168_-167del | |
NM_080871.3:c.271+154_271+155del | NP_543147.2:n.271+154_271+155del | |
NM_080871.4:c.271+154_271+155del | NP_543147.2:n.271+154_271+155del |