HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23424216_23424225del , CM000676.2:g.23424216_23424225del | GRCh38 |
NC_000014.8:g.23893425_23893434del , CM000676.1:g.23893425_23893434del | GRCh37 |
NC_000014.7:g.22963265_22963274del | NCBI36 |
NG_007884.1:g.16438_16447del , LRG_384:g.16438_16447del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2680-75_2680-66del MANE Select | ENSP00000347507.3:n.2680-75_2680-66del | |
ENST00000355349.3:c.2680-75_2680-66del | ENSP00000347507.3:n.2680-75_2680-66del | |
NM_000257.3:c.2680-75_2680-66del | NP_000248.2:n.2680-75_2680-66del | |
XR_245686.3:n.2786-75_2786-66del | ||
XM_017021340.1:c.2680-75_2680-66del | XP_016876829.1:n.2680-75_2680-66del | |
NM_000257.4:c.2680-75_2680-66del MANE Select | NP_000248.2:n.2680-75_2680-66del |