HGVS | Genome Assembly |
---|---|
NC_000006.12:g.42978539T>C , CM000668.2:g.42978539T>C | GRCh38 |
NC_000006.11:g.42946277T>C , CM000668.1:g.42946277T>C | GRCh37 |
NC_000006.10:g.43054255T>C | NCBI36 |
NG_008370.1:g.5705A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304611.13:c.612A>G MANE Select | ENSP00000303511.8:p.Ser204= | |
ENST00000244546.4:c.612A>G | ENSP00000244546.4:p.Ser204= | |
ENST00000304611.12:c.612A>G | ENSP00000303511.8:p.Ser204= | |
NM_000287.3:c.612A>G | NP_000278.3:p.Ser204= | |
NM_001316313.1:c.612A>G | NP_001303242.1:p.Ser204= | |
NR_133009.1:n.705A>G | ||
XM_011514661.1:c.612A>G | XP_011512963.1:p.Ser204= | |
XR_926246.1:n.705A>G | ||
XM_011514661.2:c.612A>G | XP_011512963.1:p.Ser204= | |
XR_001743466.2:n.1686A>G | ||
NM_000287.4:c.612A>G MANE Select | NP_000278.3:p.Ser204= | |
NM_001316313.2:c.612A>G | NP_001303242.1:p.Ser204= | |
NR_133009.2:n.643A>G |