HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153740653_153740664del , CM000685.2:g.153740653_153740664del | GRCh38 |
NC_000023.10:g.153006107_153006118del , CM000685.1:g.153006107_153006118del | GRCh37 |
NC_000023.9:g.152659301_152659312del | NCBI36 |
NG_009022.2:g.20786_20797del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1714_1725del MANE Select | ENSP00000218104.3:p.Ser572_Asp575del | |
ENST00000218104.5:c.1714_1725del | ENSP00000218104.3:p.Ser572_Asp575del | |
NM_000033.3:c.1714_1725del | NP_000024.2:p.Ser572_Asp575del | |
XR_938507.1:n.2186_2197del | ||
XR_938507.2:n.2186_2197del | ||
NM_000033.4:c.1714_1725del MANE Select | NP_000024.2:p.Ser572_Asp575del |