HGVS | Genome Assembly |
---|---|
NC_000005.10:g.93585300T>G , CM000667.2:g.93585300T>G | GRCh38 |
NC_000005.9:g.92921006T>G , CM000667.1:g.92921006T>G | GRCh37 |
NC_000005.8:g.92946762T>G | NCBI36 |
NG_034119.1:g.6964T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000615873.2:c.202T>G | ENSP00000481517.1:p.Ser68Ala | |
ENST00000327111.8:c.277T>G MANE Select | ENSP00000325819.3:p.Ser93Ala | |
ENST00000647447.1:c.124T>G | ENSP00000495740.1:p.Ser42Ala | |
ENST00000327111.7:c.277T>G | ENSP00000325819.3:p.Ser93Ala | |
ENST00000615873.1:c.202T>G | ENSP00000481517.1:p.Ser68Ala | |
NM_005654.5:c.277T>G | NP_005645.1:p.Ser93Ala | |
NM_005654.6:c.277T>G MANE Select | NP_005645.1:p.Ser93Ala |