HGVS | Genome Assembly |
---|---|
NC_000008.11:g.64624425del , CM000670.2:g.64624425del | GRCh38 |
NC_000008.10:g.65536982del , CM000670.1:g.65536982del | GRCh37 |
NC_000008.9:g.65699536del | NCBI36 |
NG_008338.1:g.179367del | |
NG_008338.2:g.179367del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310193.4:c.237del MANE Select | ENSP00000310721.3:p.Asp79GlufsTer12 | |
ENST00000310193.3:c.237del | ENSP00000310721.3:p.Asp79GlufsTer12 | |
NM_004820.3:c.237del | NP_004811.1:p.Asp79GlufsTer12 | |
NM_001324112.1:c.237del | NP_001311041.1:p.Asp79GlufsTer12 | |
NM_004820.4:c.237del | NP_004811.1:p.Asp79GlufsTer12 | |
XM_017014002.1:c.303del | XP_016869491.1:p.Asp101GlufsTer12 | |
NM_004820.5:c.237del MANE Select | NP_004811.1:p.Asp79GlufsTer12 | |
NM_001324112.2:c.237del | NP_001311041.1:p.Asp79GlufsTer12 |