HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10652620_10652626del , CM000682.2:g.10652620_10652626del | GRCh38 |
NC_000020.10:g.10633268_10633274del , CM000682.1:g.10633268_10633274del | GRCh37 |
NC_000020.9:g.10581268_10581274del | NCBI36 |
NG_007496.1:g.26422_26428del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.756-27_756-21del MANE Select | ENSP00000254958.4:n.756-27_756-21del | |
ENST00000617965.2:n.98_104del | ||
ENST00000254958.9:c.756-27_756-21del | ENSP00000254958.4:n.756-27_756-21del | |
ENST00000423891.6:n.622-27_622-21del | ||
ENST00000617965.1:n.98_104del | ||
NM_000214.2:c.756-27_756-21del | NP_000205.1:n.756-27_756-21del | |
NM_000214.3:c.756-27_756-21del MANE Select | NP_000205.1:n.756-27_756-21del |