HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339650T>G , CM000669.2:g.17339650T>G | GRCh38 |
NC_000007.13:g.17379274T>G , CM000669.1:g.17379274T>G | GRCh37 |
NC_000007.12:g.17345799T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1825T>G MANE Select | ENSP00000242057.4:p.Ser609Ala | |
ENST00000637807.1:c.1795T>G | ENSP00000490530.1:p.Ser599Ala | |
ENST00000642825.1:c.1780T>G | ENSP00000495987.1:p.Ser594Ala | |
ENST00000242057.8:c.1825T>G | ENSP00000242057.4:p.Ser609Ala | |
ENST00000463496.1:c.1825T>G | ENSP00000436466.1:p.Ser609Ala | |
NM_001621.4:c.1825T>G | NP_001612.1:p.Ser609Ala | |
NM_001621.5:c.1825T>G MANE Select | NP_001612.1:p.Ser609Ala |