HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10644663_10644664del , CM000682.2:g.10644663_10644664del | GRCh38 |
NC_000020.10:g.10625311_10625312del , CM000682.1:g.10625311_10625312del | GRCh37 |
NC_000020.9:g.10573311_10573312del | NCBI36 |
NG_007496.1:g.34384_34385del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.2344+200_2344+201del MANE Select | ENSP00000254958.4:n.2344+200_2344+201del | |
ENST00000617965.2:n.2933+200_2933+201del | ||
ENST00000254958.9:c.2344+200_2344+201del | ENSP00000254958.4:n.2344+200_2344+201del | |
ENST00000423891.6:n.2210+200_2210+201del | ||
ENST00000488480.2:n.941_942del | ||
NM_000214.2:c.2344+200_2344+201del | NP_000205.1:n.2344+200_2344+201del | |
NM_000214.3:c.2344+200_2344+201del MANE Select | NP_000205.1:n.2344+200_2344+201del |