HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23418412del , CM000676.2:g.23418412del | GRCh38 |
NC_000014.8:g.23887621del , CM000676.1:g.23887621del | GRCh37 |
NC_000014.7:g.22957461del | NCBI36 |
NG_007884.1:g.22253del , LRG_384:g.22253del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3973-3del MANE Select | ENSP00000347507.3:n.3973-3del | |
ENST00000355349.3:c.3973-3del | ENSP00000347507.3:n.3973-3del | |
NM_000257.3:c.3973-3del | NP_000248.2:n.3973-3del | |
XM_017021340.1:c.3973-3del | XP_016876829.1:n.3973-3del | |
NM_000257.4:c.3973-3del MANE Select | NP_000248.2:n.3973-3del |