HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155461310_155461313delinsCCTT , CM000669.2:g.155461310_155461313delinsCCTT | GRCh38 |
NC_000007.13:g.155254005_155254008delinsCCTT , CM000669.1:g.155254005_155254008delinsCCTT | GRCh37 |
NC_000007.12:g.154946766_154946769delinsCCTT | NCBI36 |
NG_007124.1:g.9591_9594delinsCCTT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297375.4:c.686-1061_686-1058delinsCCTT MANE Select | ENSP00000297375.4:n.686-1061_686-1058deli... | |
NM_001427.3:c.686-1061_686-1058delinsCCTT | NP_001418.2:n.686-1061_686-1058delinsCCTT... | |
NM_001427.4:c.686-1061_686-1058delinsCCTT MANE Select | NP_001418.2:n.686-1061_686-1058delinsCCTT... |