HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114230T>C , CM000667.2:g.140114230T>C | GRCh38 |
NC_000005.9:g.139493815T>C , CM000667.1:g.139493815T>C | GRCh37 |
NC_000005.8:g.139473999T>C | NCBI36 |
NG_041813.1:g.5108T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.49T>C MANE Select | ENSP00000332706.3:p.Ser17Pro | |
ENST00000505703.2:c.49T>C | ENSP00000498560.1:p.Ser17Pro | |
ENST00000651386.1:c.49T>C | ENSP00000499133.1:p.Ser17Pro | |
ENST00000331327.4:c.49T>C | ENSP00000332706.3:p.Ser17Pro | |
ENST00000502351.1:n.472T>C | ||
ENST00000505703.1:n.514T>C | ||
NM_005859.4:c.49T>C | NP_005850.1:p.Ser17Pro | |
NM_005859.5:c.49T>C MANE Select | NP_005850.1:p.Ser17Pro |