HGVS | Genome Assembly |
---|---|
NC_000011.10:g.13974462_13974464del , CM000673.2:g.13974462_13974464del | GRCh38 |
NC_000011.9:g.13996009_13996011del , CM000673.1:g.13996009_13996011del | GRCh37 |
NC_000011.8:g.13952585_13952587del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000576479.4:c.239-8385_239-8383del MANE Select | ENSP00000460236.1:n.239-8385_239-8383del | |
ENST00000576479.3:c.239-8385_239-8383del | ENSP00000460236.1:n.239-8385_239-8383del | |
NM_006108.3:c.239-8385_239-8383del | NP_006099.2:n.239-8385_239-8383del | |
NM_006108.4:c.239-8385_239-8383del MANE Select | NP_006099.2:n.239-8385_239-8383del |