HGVS | Genome Assembly |
---|---|
NC_000006.12:g.143485236T>A , CM000668.2:g.143485236T>A | GRCh38 |
NC_000006.11:g.143806373T>A , CM000668.1:g.143806373T>A | GRCh37 |
NC_000006.10:g.143848066T>A | NCBI36 |
NG_008459.1:g.39456T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367591.5:c.1026T>A MANE Select | ENSP00000356563.4:p.Ser342Arg | |
ENST00000367591.4:c.1026T>A | ENSP00000356563.4:p.Ser342Arg | |
ENST00000585848.1:n.165T>A | ||
NM_003630.2:c.1026T>A | NP_003621.1:p.Ser342Arg | |
NM_003630.3:c.1026T>A MANE Select | NP_003621.1:p.Ser342Arg |