HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339804T>G , CM000669.2:g.17339804T>G | GRCh38 |
NC_000007.13:g.17379428T>G , CM000669.1:g.17379428T>G | GRCh37 |
NC_000007.12:g.17345953T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1979T>G MANE Select | ENSP00000242057.4:p.Val660Gly | |
ENST00000637807.1:c.1949T>G | ENSP00000490530.1:p.Val650Gly | |
ENST00000642825.1:c.1934T>G | ENSP00000495987.1:p.Val645Gly | |
ENST00000242057.8:c.1979T>G | ENSP00000242057.4:p.Val660Gly | |
ENST00000463496.1:c.1979T>G | ENSP00000436466.1:p.Val660Gly | |
NM_001621.4:c.1979T>G | NP_001612.1:p.Val660Gly | |
NM_001621.5:c.1979T>G MANE Select | NP_001612.1:p.Val660Gly |