HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713650_6713652del , CM000681.2:g.6713650_6713652del | GRCh38 |
NC_000019.9:g.6713661_6713663del , CM000681.1:g.6713661_6713663del | GRCh37 |
NC_000019.8:g.6664661_6664663del | NCBI36 |
NG_009557.1:g.12000_12002del , LRG_27:g.12000_12002del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.651-143_651-141del | ENSP00000512083.1:n.651-143_651-141del | |
ENST00000245907.11:c.774-143_774-141del MANE Select | ENSP00000245907.4:n.774-143_774-141del | |
ENST00000245907.10:c.774-143_774-141del | ENSP00000245907.4:n.774-143_774-141del | |
ENST00000595577.1:n.278-143_278-141del | ||
ENST00000597442.5:n.23+114_23+116del | ||
NM_000064.3:c.774-143_774-141del | NP_000055.2:n.774-143_774-141del | |
NM_000064.4:c.774-143_774-141del MANE Select | NP_000055.2:n.774-143_774-141del |