HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420844_23420863del , CM000676.2:g.23420844_23420863del | GRCh38 |
NC_000014.8:g.23890053_23890072del , CM000676.1:g.23890053_23890072del | GRCh37 |
NC_000014.7:g.22959893_22959912del | NCBI36 |
NG_007884.1:g.19802_19821del , LRG_384:g.19802_19821del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3336+98_3336+117del MANE Select | ENSP00000347507.3:n.3336+98_3336+117del | |
ENST00000355349.3:c.3336+98_3336+117del | ENSP00000347507.3:n.3336+98_3336+117del | |
NM_000257.3:c.3336+98_3336+117del | NP_000248.2:n.3336+98_3336+117del | |
XR_245686.3:n.3444+98_3444+117del | ||
XM_017021340.1:c.3336+98_3336+117del | XP_016876829.1:n.3336+98_3336+117del | |
NM_000257.4:c.3336+98_3336+117del MANE Select | NP_000248.2:n.3336+98_3336+117del |