HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978159C>T , CM000667.2:g.149978159C>T | GRCh38 |
NC_000005.9:g.149357722C>T , CM000667.1:g.149357722C>T | GRCh37 |
NC_000005.8:g.149337915C>T | NCBI36 |
NG_007147.2:g.19277C>T , LRG_684:g.19277C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000690410.1:n.739C>T | ||
ENST00000286298.5:c.507C>T MANE Select | ENSP00000286298.4:p.Cys169= | |
ENST00000286298.4:c.507C>T | ENSP00000286298.4:p.Cys169= | |
ENST00000503336.1:c.180C>T | ENSP00000426053.1:p.Cys60= | |
NM_000112.3:c.507C>T , LRG_684t1:c.507C>T | NP_000103.2:p.Cys169= | |
XM_017009191.2:c.507C>T | XP_016864680.1:p.Cys169= | |
NM_000112.4:c.507C>T MANE Select | NP_000103.2:p.Cys169= |