HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35845984_35845985del , CM000681.2:g.35845984_35845985del | GRCh38 |
NC_000019.9:g.36336886_36336887del , CM000681.1:g.36336886_36336887del | GRCh37 |
NC_000019.8:g.41028726_41028727del | NCBI36 |
NG_013356.2:g.28304_28305del , LRG_693:g.28304_28305del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1627+24_1627+25del MANE Select | ENSP00000368190.4:n.1627+24_1627+25del | |
ENST00000353632.6:c.1627+24_1627+25del | ENSP00000343634.5:n.1627+24_1627+25del | |
ENST00000378910.9:c.1627+24_1627+25del | ENSP00000368190.4:n.1627+24_1627+25del | |
NM_004646.3:c.1627+24_1627+25del , LRG_693t1:c.1627+24_1627+25del | NP_004637.1:n.1627+24_1627+25del | |
NM_004646.4:c.1627+24_1627+25del MANE Select | NP_004637.1:n.1627+24_1627+25del |