HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420869_23420870insCA , CM000676.2:g.23420869_23420870insCA | GRCh38 |
NC_000014.8:g.23890078_23890079insCA , CM000676.1:g.23890078_23890079insCA | GRCh37 |
NC_000014.7:g.22959918_22959919insCA | NCBI36 |
NG_007884.1:g.19792_19793insTG , LRG_384:g.19792_19793insTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3336+88_3336+89insTG MANE Select | ENSP00000347507.3:n.3336+88_3336+89insTG | |
ENST00000355349.3:c.3336+88_3336+89insTG | ENSP00000347507.3:n.3336+88_3336+89insTG | |
NM_000257.3:c.3336+88_3336+89insTG | NP_000248.2:n.3336+88_3336+89insTG | |
XR_245686.3:n.3444+88_3444+89insTG | ||
XM_017021340.1:c.3336+88_3336+89insTG | XP_016876829.1:n.3336+88_3336+89insTG | |
NM_000257.4:c.3336+88_3336+89insTG MANE Select | NP_000248.2:n.3336+88_3336+89insTG |