HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2317782del , CM000678.2:g.2317782del | GRCh38 |
NC_000016.9:g.2367783del , CM000678.1:g.2367783del | GRCh37 |
NC_000016.8:g.2307784del | NCBI36 |
NG_011790.1:g.27965del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301732.10:c.874-18del MANE Select | ENSP00000301732.5:n.874-18del | |
ENST00000301732.9:c.874-18del | ENSP00000301732.5:n.874-18del | |
ENST00000382381.7:c.874-18del | ENSP00000371818.3:n.874-18del | |
ENST00000563623.5:n.1437-18del | ||
NM_001089.2:c.874-18del | NP_001080.2:n.874-18del | |
NM_001089.3:c.874-18del MANE Select | NP_001080.2:n.874-18del |