HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23413887del , CM000676.2:g.23413887del | GRCh38 |
NC_000014.8:g.23883096del , CM000676.1:g.23883096del | GRCh37 |
NC_000014.7:g.22952936del | NCBI36 |
NG_007884.1:g.26775del , LRG_384:g.26775del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.5662del MANE Select | ENSP00000347507.3:p.Gln1888LysfsTer? | |
ENST00000355349.3:c.5662del | ENSP00000347507.3:p.Gln1888LysfsTer? | |
NM_000257.3:c.5662del | NP_000248.2:p.Gln1888LysfsTer? | |
XM_017021340.1:c.5662del | XP_016876829.1:p.Gln1888LysfsTer? | |
NM_000257.4:c.5662del MANE Select | NP_000248.2:p.Gln1888LysfsTer? |