HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423441_23423442insAA , CM000676.2:g.23423441_23423442insAA | GRCh38 |
NC_000014.8:g.23892650_23892651insAA , CM000676.1:g.23892650_23892651insAA | GRCh37 |
NC_000014.7:g.22962490_22962491insAA | NCBI36 |
NG_007884.1:g.17221_17222insTT , LRG_384:g.17221_17222insTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+106_3099+107insTT MANE Select | ENSP00000347507.3:n.3099+106_3099+107insTT | |
ENST00000355349.3:c.3099+106_3099+107insTT | ENSP00000347507.3:n.3099+106_3099+107insTT | |
NM_000257.3:c.3099+106_3099+107insTT | NP_000248.2:n.3099+106_3099+107insTT | |
XR_245686.3:n.3205+106_3205+107insTT | ||
XM_017021340.1:c.3099+106_3099+107insTT | XP_016876829.1:n.3099+106_3099+107insTT | |
NM_000257.4:c.3099+106_3099+107insTT MANE Select | NP_000248.2:n.3099+106_3099+107insTT |