HGVS | Genome Assembly |
---|---|
NC_000023.11:g.68829891T>G , CM000685.2:g.68829891T>G | GRCh38 |
NC_000023.10:g.68049734T>G , CM000685.1:g.68049734T>G | GRCh37 |
NC_000023.9:g.67966459T>G | NCBI36 |
NG_008887.1:g.5895T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000204961.5:c.115T>G MANE Select | ENSP00000204961.4:p.Ser39Ala | |
ENST00000204961.4:c.115T>G | ENSP00000204961.4:p.Ser39Ala | |
NM_004429.4:c.115T>G | NP_004420.1:p.Ser39Ala | |
NM_004429.5:c.115T>G MANE Select | NP_004420.1:p.Ser39Ala |