HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48419674dup , CM000681.2:g.48419674dup | GRCh38 |
NC_000019.9:g.48922931dup , CM000681.1:g.48922931dup | GRCh37 |
NC_000019.8:g.53614743dup | NCBI36 |
NG_052829.1:g.29800dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263269.4:c.1951dup MANE Select | ENSP00000263269.2:p.Arg651ProfsTer? | |
ENST00000263269.3:c.1951dup | ENSP00000263269.2:p.Arg651ProfsTer? | |
NM_000836.2:c.1951dup | NP_000827.2:p.Arg651ProfsTer? | |
XM_011526872.1:c.1951dup | XP_011525174.1:p.Arg651ProfsTer? | |
NM_000836.4:c.1951dup MANE Select | NP_000827.2:p.Arg651ProfsTer? |