HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96251035G>T , CM000664.2:g.96251035G>T | GRCh38 |
NC_000002.11:g.96916773G>T , CM000664.1:g.96916773G>T | GRCh37 |
NC_000002.10:g.96280500G>T | NCBI36 |
NG_027695.1:g.19979C>A , LRG_528:g.19979C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258439.8:c.*2773C>A MANE Select | ENSP00000258439.3:n.*2773C>A | |
ENST00000258439.7:c.*2773C>A | ENSP00000258439.2:n.*2773C>A | |
NM_001193304.2:c.*2773C>A | NP_001180233.1:n.*2773C>A | |
NM_017849.3:c.*2773C>A , LRG_528t1:c.*2773C>A | NP_060319.1:n.*2773C>A | |
XM_017004450.1:c.*2074C>A | XP_016859939.1:n.*2074C>A | |
XM_017004452.1:c.*2773C>A | XP_016859941.1:n.*2773C>A | |
NM_001193304.3:c.*2773C>A | NP_001180233.1:n.*2773C>A | |
NM_017849.4:c.*2773C>A MANE Select | NP_060319.1:n.*2773C>A |