HGVS | Genome Assembly |
---|---|
NC_000010.11:g.30314109_30314128del , CM000672.2:g.30314109_30314128del | GRCh38 |
NC_000010.10:g.30603038_30603057del , CM000672.1:g.30603038_30603057del | GRCh37 |
NC_000010.9:g.30643044_30643063del | NCBI36 |
NG_028096.1:g.40213_40232del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263063.9:c.1387-155_1387-136del MANE Select | ENSP00000263063.3:n.1387-155_1387-136del | |
ENST00000263063.8:c.1387-155_1387-136del | ENSP00000263063.3:n.1387-155_1387-136del | |
ENST00000488290.5:n.3142-155_3142-136del | ||
NM_018109.3:c.1387-155_1387-136del | NP_060579.3:n.1387-155_1387-136del | |
NM_018109.4:c.1387-155_1387-136del MANE Select | NP_060579.3:n.1387-155_1387-136del |