HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750989A>C , CM000684.2:g.27750989A>C | GRCh38 |
NC_000022.10:g.28146977A>C , CM000684.1:g.28146977A>C | GRCh37 |
NC_000022.9:g.26476977A>C | NCBI36 |
NG_023258.1:g.55510T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.414T>G | ||
ENST00000302326.5:c.3889T>G MANE Select | ENSP00000304956.4:p.Ser1297Ala | |
ENST00000302326.4:c.3889T>G | ENSP00000304956.4:p.Ser1297Ala | |
ENST00000424656.1:c.242T>G | ||
ENST00000497225.1:n.245T>G | ||
NM_002430.2:c.3889T>G | NP_002421.3:p.Ser1297Ala | |
NM_002430.3:c.3889T>G MANE Select | NP_002421.3:p.Ser1297Ala |