HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242417G= , CM000684.2:g.20242417G= | GRCh38 |
NC_000022.10:g.20229940G= , CM000684.1:g.20229940G= | GRCh37 |
NC_000022.9:g.18609940G= | NCBI36 |
NG_012176.1:g.30877C= | |
NG_012176.2:g.30877C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.716C= MANE Select | ENSP00000043402.7:p.Ser239= | |
ENST00000043402.7:c.716C= | ENSP00000043402.7:p.Ser239= | |
ENST00000416372.5:c.775C= | ||
ENST00000425986.1:c.973C= | ||
NM_023004.5:c.716C= | NP_075380.1:p.Ser239= | |
NM_023004.6:c.716C= MANE Select | NP_075380.1:p.Ser239= |