HGVS | Genome Assembly |
---|---|
NC_000018.10:g.21815724C= , CM000680.2:g.21815724C= | GRCh38 |
NC_000018.9:g.19395685C= , CM000680.1:g.19395685C= | GRCh37 |
NC_000018.8:g.17649683C= | NCBI36 |
NG_033272.2:g.115768C= , LRG_759:g.115768C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261537.7:c.1588C= MANE Select | ENSP00000261537.6:p.Arg530= | |
ENST00000261537.6:c.1588C= | ENSP00000261537.6:p.Arg530= | |
ENST00000577749.5:n.573C= | ||
ENST00000578260.1:n.391C= | ||
ENST00000578646.5:n.1565C= | ||
NM_020774.3:c.1588C= , LRG_759t1:c.1588C= | NP_065825.1:p.Arg530= | |
XM_011526098.1:c.118C= | XP_011524400.1:p.Arg40= | |
XM_017025873.1:c.1072C= | XP_016881362.1:p.Arg358= | |
NM_020774.4:c.1588C= MANE Select | NP_065825.1:p.Arg530= |