HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29072955_29072957del , CM000664.2:g.29072955_29072957del | GRCh38 |
NC_000002.11:g.29295821_29295823del , CM000664.1:g.29295821_29295823del | GRCh37 |
NC_000002.10:g.29149325_29149327del | NCBI36 |
NG_021427.1:g.6306_6308del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.1306_1308del MANE Select | ENSP00000332809.4:p.Ser436del | |
ENST00000331664.5:c.1306_1308del | ENSP00000332809.4:p.Ser436del | |
NM_001029883.2:c.1306_1308del | NP_001025054.1:p.Ser436del | |
XM_011532826.1:c.1306_1308del | XP_011531128.1:p.Ser436del | |
XR_939901.1:n.185+3788_185+3790del | ||
XR_939902.1:n.173+3800_173+3802del | ||
NM_001029883.3:c.1306_1308del MANE Select | NP_001025054.1:p.Ser436del |