HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23422504_23422505delinsCA , CM000676.2:g.23422504_23422505delinsCA | GRCh38 |
NC_000014.8:g.23891713_23891714delinsCA , CM000676.1:g.23891713_23891714delinsCA | GRCh37 |
NC_000014.7:g.22961553_22961554delinsCA | NCBI36 |
NG_007884.1:g.18157_18158delinsTG , LRG_384:g.18157_18158delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3100-180_3100-179delinsTG MANE Select | ENSP00000347507.3:n.3100-180_3100-179delinsTG | |
ENST00000355349.3:c.3100-180_3100-179delinsTG | ENSP00000347507.3:n.3100-180_3100-179delinsTG | |
NM_000257.3:c.3100-180_3100-179delinsTG | NP_000248.2:n.3100-180_3100-179delinsTG | |
XR_245686.3:n.3206-180_3206-179delinsTG | ||
XM_017021340.1:c.3100-180_3100-179delinsTG | XP_016876829.1:n.3100-180_3100-179delinsTG | |
NM_000257.4:c.3100-180_3100-179delinsTG MANE Select | NP_000248.2:n.3100-180_3100-179delinsTG |