HGVS | Genome Assembly |
---|---|
NC_000002.12:g.208124088del , CM000664.2:g.208124088del | GRCh38 |
NC_000002.11:g.208988812del , CM000664.1:g.208988812del | GRCh37 |
NC_000002.10:g.208697057del | NCBI36 |
NG_008039.1:g.5504del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264376.5:c.252+26del MANE Select | ENSP00000264376.4:n.252+26del | |
ENST00000264376.4:c.252+26del | ENSP00000264376.4:n.252+26del | |
NM_006891.3:c.252+26del | NP_008822.2:n.252+26del | |
NR_038437.1:n.97+4863del | ||
NM_006891.4:c.252+26del MANE Select | NP_008822.2:n.252+26del |