HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74763440C>G , CM000679.2:g.74763440C>G | GRCh38 |
NC_000017.10:g.72759579C>G , CM000679.1:g.72759579C>G | GRCh37 |
NC_000017.9:g.70271174C>G | NCBI36 |
NG_013022.1:g.19817C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262613.10:c.677C>G MANE Select | ENSP00000262613.5:p.Thr226Ser | |
ENST00000262613.9:c.677C>G | ENSP00000262613.5:p.Thr226Ser | |
ENST00000413388.2:c.209C>G | ENSP00000464982.1:p.Thr70Ser | |
ENST00000578958.1:n.411C>G | ||
ENST00000581356.1:c.13C>G | ||
ENST00000583369.5:c.442-4707C>G | ENSP00000464321.1:n.442-4707C>G | |
NM_004252.4:c.677C>G | NP_004243.1:p.Thr226Ser | |
XR_002958087.1:n.896C>G | ||
NM_004252.5:c.677C>G MANE Select | NP_004243.1:p.Thr226Ser |