HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420819_23420820delinsCT , CM000676.2:g.23420819_23420820delinsCT | GRCh38 |
NC_000014.8:g.23890028_23890029delinsCT , CM000676.1:g.23890028_23890029delinsCT | GRCh37 |
NC_000014.7:g.22959868_22959869delinsCT | NCBI36 |
NG_007884.1:g.19842_19843delinsAG , LRG_384:g.19842_19843delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3336+138_3336+139delinsAG MANE Select | ENSP00000347507.3:n.3336+138_3336+139delinsAG | |
ENST00000355349.3:c.3336+138_3336+139delinsAG | ENSP00000347507.3:n.3336+138_3336+139delinsAG | |
NM_000257.3:c.3336+138_3336+139delinsAG | NP_000248.2:n.3336+138_3336+139delinsAG | |
XR_245686.3:n.3444+138_3444+139delinsAG | ||
XM_017021340.1:c.3336+138_3336+139delinsAG | XP_016876829.1:n.3336+138_3336+139delinsAG | |
NM_000257.4:c.3336+138_3336+139delinsAG MANE Select | NP_000248.2:n.3336+138_3336+139delinsAG |