HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154902019_154902021delinsGGT , CM000685.2:g.154902019_154902021delinsGGT | GRCh38 |
NC_000023.10:g.154130294_154130296delinsGGT , CM000685.1:g.154130294_154130296delinsGGT | GRCh37 |
NC_000023.9:g.153783488_153783490delinsGGT | NCBI36 |
NG_011403.1:g.125703_125705delinsACC | |
NG_011403.2:g.125703_125705delinsACC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.6115+30_6115+32delinsACC MANE Select | ENSP00000353393.4:n.6115+30_6115+32delins... | |
ENST00000360256.8:c.6115+30_6115+32delinsACC | ENSP00000353393.4:n.6115+30_6115+32delins... | |
NM_000132.3:c.6115+30_6115+32delinsACC | NP_000123.1:n.6115+30_6115+32delinsACC | |
XM_011531126.1:c.6010+30_6010+32delinsACC | XP_011529428.1:n.6010+30_6010+32delinsACC... | |
NM_000132.4:c.6115+30_6115+32delinsACC MANE Select | NP_000123.1:n.6115+30_6115+32delinsACC |