HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2251909C>A , CM000681.2:g.2251909C>A | GRCh38 |
NC_000019.9:g.2251908C>A , CM000681.1:g.2251908C>A | GRCh37 |
NC_000019.8:g.2202908C>A | NCBI36 |
NG_012190.1:g.7796C>A | |
NG_032853.1:g.9515G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221496.5:c.1635C>A MANE Select | ENSP00000221496.2:p.Ser545Arg | |
ENST00000221496.4:c.1635C>A | ENSP00000221496.2:p.Ser545Arg | |
NM_000479.3:c.1635C>A | NP_000470.2:p.Ser545Arg | |
NM_000479.4:c.1635C>A | NP_000470.2:p.Ser545Arg | |
NM_000479.5:c.1635C>A MANE Select | NP_000470.3:p.Ser545Arg |