HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10115480T>C , CM000681.2:g.10115480T>C | GRCh38 |
NC_000019.9:g.10226156T>C , CM000681.1:g.10226156T>C | GRCh37 |
NC_000019.8:g.10087156T>C | NCBI36 |
NG_047007.1:g.8960T>C | |
NG_051197.1:g.9445A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253108.9:c.946A>G MANE Select | ENSP00000253108.3:p.Lys316Glu | |
ENST00000253108.8:c.946A>G | ENSP00000253108.3:p.Lys316Glu | |
ENST00000590158.1:n.965A>G | ||
ENST00000593054.5:c.340A>G | ENSP00000467187.1:p.Lys114Glu | |
NM_003755.3:c.946A>G | NP_003746.2:p.Lys316Glu | |
NM_003755.4:c.946A>G | NP_003746.2:p.Lys316Glu | |
NM_003755.5:c.946A>G MANE Select | NP_003746.2:p.Lys316Glu |