HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780423_94780433del , CM000672.2:g.94780423_94780433del | GRCh38 |
NC_000010.10:g.96540180_96540190del , CM000672.1:g.96540180_96540190del | GRCh37 |
NC_000010.9:g.96530170_96530180del | NCBI36 |
NG_008384.2:g.22718_22728del | |
NG_008384.3:g.22743_22753del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.482-76_482-66del MANE Select | ENSP00000360372.3:n.482-76_482-66del | |
ENST00000645461.1:n.1535-76_1535-66del | ||
ENST00000371321.7:c.482-76_482-66del | ENSP00000360372.3:n.482-76_482-66del | |
ENST00000464755.1:c.1245-76_1245-66del | ENSP00000483243.1:n.1245-76_1245-66del | |
NM_000769.2:c.482-76_482-66del | NP_000760.1:n.482-76_482-66del | |
NM_000769.4:c.482-76_482-66del MANE Select | NP_000760.1:n.482-76_482-66del |