HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240869159_240869162delinsTGCATGCAAGAT , CM000664.2:g.240869159_240869162delinsTGCATGCAAGAT | GRCh38 |
NC_000002.11:g.241808576_241808579delinsTGCATGCAAGAT , CM000664.1:g.241808576_241808579delinsTGCATGCAAGAT | GRCh37 |
NC_000002.10:g.241457249_241457252delinsTGCATGCAAGAT | NCBI36 |
NG_008005.1:g.5415_5418delinsTGCATGCAAGAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.166-11_166-8delinsTGCATGCAAGAT MANE Select | ENSP00000302620.3:n.166-11_166-8delinsTGC... | |
ENST00000307503.3:c.166-11_166-8delinsTGCATGCAAGAT | ENSP00000302620.3:n.166-11_166-8delinsTGC... | |
ENST00000472436.1:n.186-11_186-8delinsTGCATGCAAGAT | ||
NM_000030.2:c.166-11_166-8delinsTGCATGCAAGAT | NP_000021.1:n.166-11_166-8delinsTGCATGCAA... | |
XR_924060.1:n.405+1071_405+1074delinsATCTTGCATGCA | ||
NM_000030.3:c.166-11_166-8delinsTGCATGCAAGAT MANE Select | NP_000021.1:n.166-11_166-8delinsTGCATGCAA... |