HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339568C>G , CM000669.2:g.17339568C>G | GRCh38 |
NC_000007.13:g.17379192C>G , CM000669.1:g.17379192C>G | GRCh37 |
NC_000007.12:g.17345717C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1743C>G MANE Select | ENSP00000242057.4:p.Ile581Met | |
ENST00000637807.1:c.1713C>G | ENSP00000490530.1:p.Ile571Met | |
ENST00000642825.1:c.1698C>G | ENSP00000495987.1:p.Ile566Met | |
ENST00000242057.8:c.1743C>G | ENSP00000242057.4:p.Ile581Met | |
ENST00000463496.1:c.1743C>G | ENSP00000436466.1:p.Ile581Met | |
NM_001621.4:c.1743C>G | NP_001612.1:p.Ile581Met | |
NM_001621.5:c.1743C>G MANE Select | NP_001612.1:p.Ile581Met |