HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339717T>G , CM000669.2:g.17339717T>G | GRCh38 |
NC_000007.13:g.17379341T>G , CM000669.1:g.17379341T>G | GRCh37 |
NC_000007.12:g.17345866T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1892T>G MANE Select | ENSP00000242057.4:p.Val631Gly | |
ENST00000637807.1:c.1862T>G | ENSP00000490530.1:p.Val621Gly | |
ENST00000642825.1:c.1847T>G | ENSP00000495987.1:p.Val616Gly | |
ENST00000242057.8:c.1892T>G | ENSP00000242057.4:p.Val631Gly | |
ENST00000463496.1:c.1892T>G | ENSP00000436466.1:p.Val631Gly | |
NM_001621.4:c.1892T>G | NP_001612.1:p.Val631Gly | |
NM_001621.5:c.1892T>G MANE Select | NP_001612.1:p.Val631Gly |