HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42404797G>T , CM000679.2:g.42404797G>T | GRCh38 |
NC_000017.10:g.40556815G>T , CM000679.1:g.40556815G>T | GRCh37 |
NC_000017.9:g.37810341G>T | NCBI36 |
NG_015845.1:g.23524C>A | |
NG_015845.2:g.23524C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357037.6:c.1063C>A MANE Select | ENSP00000349541.4:p.Arg355Ser | |
ENST00000357037.5:c.1063C>A | ENSP00000349541.4:p.Arg355Ser | |
NM_012232.5:c.1063C>A | NP_036364.2:p.Arg355Ser | |
NM_012232.6:c.1063C>A MANE Select | NP_036364.2:p.Arg355Ser |