HGVS | Genome Assembly |
---|---|
NC_000017.11:g.66228259_66228260delinsGC , CM000679.2:g.66228259_66228260delinsGC | GRCh38 |
NC_000017.10:g.64224377_64224378delinsGC , CM000679.1:g.64224377_64224378delinsGC | GRCh37 |
NC_000017.9:g.61654839_61654840delinsGC | NCBI36 |
NG_012045.1:g.6179_6180delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000205948.11:c.65-64_65-63delinsGC MANE Select | ENSP00000205948.6:n.65-64_65-63delinsGC | |
ENST00000205948.10:c.65-64_65-63delinsGC | ENSP00000205948.6:n.65-64_65-63delinsGC | |
ENST00000577982.1:c.65-64_65-63delinsGC | ENSP00000464301.1:n.65-64_65-63delinsGC | |
ENST00000581797.5:c.-116-64_-116-63delinsGC | ENSP00000463553.1:n.-116-64_-116-63delinsGC | |
NM_000042.2:c.65-64_65-63delinsGC | NP_000033.2:n.65-64_65-63delinsGC | |
NM_000042.3:c.65-64_65-63delinsGC MANE Select | NP_000033.2:n.65-64_65-63delinsGC |