HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32814368A>C , CM000668.2:g.32814368A>C | GRCh38 |
NC_000006.11:g.32782145A>C , CM000668.1:g.32782145A>C | GRCh37 |
NC_000006.10:g.32890123A>C | NCBI36 |
NG_009793.3:g.29403T>G | |
NG_012008.1:g.7681T>G | |
NG_009793.4:g.29403T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000438763.7:c.595T>G MANE Select | ENSP00000390020.2:p.Cys199Gly | |
ENST00000648009.1:c.595T>G | ENSP00000496848.1:p.Cys199Gly | |
ENST00000438763.6:c.595T>G | ENSP00000390020.2:p.Cys199Gly | |
ENST00000452392.2:c.2416T>G | ENSP00000391806.2:p.Cys806Gly | |
ENST00000475235.1:n.632T>G | ||
ENST00000488325.5:c.*366T>G | ENSP00000436618.1:n.*366T>G | |
NM_002120.3:c.595T>G | NP_002111.1:p.Cys199Gly | |
NM_002120.4:c.595T>G MANE Select | NP_002111.1:p.Cys199Gly |