HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008148_88008149delinsCG , CM000666.2:g.88008148_88008149delinsCG | GRCh38 |
NC_000004.11:g.88929300_88929301delinsCG , CM000666.1:g.88929300_88929301delinsCG | GRCh37 |
NC_000004.10:g.89148324_89148325delinsCG | NCBI36 |
NG_008604.1:g.5481_5482delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.415_416delinsCG MANE Select | ENSP00000237596.2:p.Arg139= | |
ENST00000237596.6:c.415_416delinsCG | ENSP00000237596.2:p.Arg139= | |
NM_000297.3:c.415_416delinsCG | NP_000288.1:p.Arg139= | |
XM_011532028.1:c.415_416delinsCG | XP_011530330.1:p.Arg139= | |
XR_244632.2:n.510_511delinsCG | ||
NR_156488.1:n.502_503delinsCG | ||
XM_011532028.2:c.415_416delinsCG | XP_011530330.1:p.Arg139= | |
NM_000297.4:c.415_416delinsCG MANE Select | NP_000288.1:p.Arg139= | |
NR_156488.2:n.514_515delinsCG |