HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713602_6713603del , CM000681.2:g.6713602_6713603del | GRCh38 |
NC_000019.9:g.6713613_6713614del , CM000681.1:g.6713613_6713614del | GRCh37 |
NC_000019.8:g.6664613_6664614del | NCBI36 |
NG_009557.1:g.12052_12053del , LRG_27:g.12052_12053del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.651-91_651-90del | ENSP00000512083.1:n.651-91_651-90del | |
ENST00000695692.1:n.7_8del | ||
ENST00000245907.11:c.774-91_774-90del MANE Select | ENSP00000245907.4:n.774-91_774-90del | |
ENST00000245907.10:c.774-91_774-90del | ENSP00000245907.4:n.774-91_774-90del | |
ENST00000595577.1:n.278-91_278-90del | ||
ENST00000597442.5:n.24-91_24-90del | ||
NM_000064.3:c.774-91_774-90del | NP_000055.2:n.774-91_774-90del | |
NM_000064.4:c.774-91_774-90del MANE Select | NP_000055.2:n.774-91_774-90del |