HGVS | Genome Assembly |
---|---|
NC_000020.11:g.59024379del , CM000682.2:g.59024379del | GRCh38 |
NC_000020.10:g.57599434del , CM000682.1:g.57599434del | GRCh37 |
NC_000020.9:g.57032829del | NCBI36 |
NG_023424.2:g.10126del , LRG_581:g.10126del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000217133.2:c.952del MANE Select | ENSP00000217133.1:p.Arg318GlyfsTer? | |
ENST00000217133.1:c.952del | ENSP00000217133.1:p.Arg318GlyfsTer? | |
NM_030773.3:c.952del , LRG_581t1:c.952del | NP_110400.1:p.Arg318GlyfsTer? | |
XM_017028085.1:c.886del | XP_016883574.1:p.Arg296GlyfsTer? | |
NM_030773.4:c.952del MANE Select | NP_110400.1:p.Arg318GlyfsTer? |