HGVS | Genome Assembly |
---|---|
NC_000007.14:g.151187310_151187311del , CM000669.2:g.151187310_151187311del | GRCh38 |
NC_000007.13:g.150884397_150884398del , CM000669.1:g.150884397_150884398del | GRCh37 |
NC_000007.12:g.150515330_150515331del | NCBI36 |
NG_017016.1:g.5522_5523del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000275838.5:c.-181_-180del | ENSP00000275838.1:n.-181_-180del | |
ENST00000377867.7:c.271+141_271+142del | ENSP00000367098.3:n.271+141_271+142del | |
ENST00000415615.1:c.*64_*65del | ENSP00000410871.1:n.*64_*65del | |
NM_001142459.1:c.-181_-180del | NP_001135931.2:n.-181_-180del | |
NM_001142460.1:c.-181_-180del | NP_001135932.2:n.-181_-180del | |
NM_080871.3:c.271+141_271+142del | NP_543147.2:n.271+141_271+142del | |
NM_080871.4:c.271+141_271+142del | NP_543147.2:n.271+141_271+142del |