HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31598640T= , CM000680.2:g.31598640T= | GRCh38 |
NC_000018.9:g.29178603T= , CM000680.1:g.29178603T= | GRCh37 |
NC_000018.8:g.27432601T= | NCBI36 |
NG_009490.1:g.11874T= , LRG_416:g.11874T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000237014.8:c.409T= MANE Select | ENSP00000237014.4:p.Ser137= | |
ENST00000610404.5:c.313T= | ENSP00000477599.2:p.Ser105= | |
ENST00000649620.1:c.409T= | ENSP00000497927.1:p.Ser137= | |
ENST00000237014.7:c.409T= | ENSP00000237014.3:p.Ser137= | |
ENST00000610404.4:c.523T= | ENSP00000477599.1:p.Ser175= | |
ENST00000613781.1:c.385T= | ENSP00000479174.1:p.Ser129= | |
NM_000371.3:c.409T= , LRG_416t1:c.409T= | NP_000362.1:p.Ser137= | |
NM_000371.4:c.409T= MANE Select | NP_000362.1:p.Ser137= |