HGVS | Genome Assembly |
---|---|
NC_000023.11:g.21845352T>C , CM000685.2:g.21845352T>C | GRCh38 |
NC_000023.10:g.21863470T>C , CM000685.1:g.21863470T>C | GRCh37 |
NC_000023.9:g.21773391T>C | NCBI36 |
NG_012797.1:g.10815T>C | |
NG_012797.2:g.10815T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379484.10:c.406T>C MANE Select | ENSP00000368798.5:p.Ser136Pro | |
ENST00000365779.2:c.406T>C | ENSP00000368796.1:p.Ser136Pro | |
ENST00000379484.9:c.406T>C | ENSP00000368798.5:p.Ser136Pro | |
ENST00000465888.1:n.505T>C | ||
NM_015884.3:c.406T>C | NP_056968.1:p.Ser136Pro | |
NM_015884.4:c.406T>C MANE Select | NP_056968.1:p.Ser136Pro |