HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155461306_155461307delinsGC , CM000669.2:g.155461306_155461307delinsGC | GRCh38 |
NC_000007.13:g.155254001_155254002delinsGC , CM000669.1:g.155254001_155254002delinsGC | GRCh37 |
NC_000007.12:g.154946762_154946763delinsGC | NCBI36 |
NG_007124.1:g.9587_9588delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297375.4:c.686-1065_686-1064delinsGC MANE Select | ENSP00000297375.4:n.686-1065_686-1064deli... | |
NM_001427.3:c.686-1065_686-1064delinsGC | NP_001418.2:n.686-1065_686-1064delinsGC | |
NM_001427.4:c.686-1065_686-1064delinsGC MANE Select | NP_001418.2:n.686-1065_686-1064delinsGC |