HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119414219T>G , CM000665.2:g.119414219T>G | GRCh38 |
NC_000003.11:g.119133066T>G , CM000665.1:g.119133066T>G | GRCh37 |
NC_000003.10:g.120615756T>G | NCBI36 |
NG_007665.2:g.124847T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.2290T>G MANE Select | ENSP00000264245.4:p.Ser764Ala | |
ENST00000264245.8:c.2290T>G | ENSP00000264245.4:p.Ser764Ala | |
NM_020754.3:c.2290T>G | NP_065805.2:p.Ser764Ala | |
XM_005247671.3:c.2197T>G | XP_005247728.1:p.Ser733Ala | |
XM_006713714.2:c.2230T>G | XP_006713777.1:p.Ser744Ala | |
XM_006713714.3:c.2230T>G | XP_006713777.1:p.Ser744Ala | |
XM_017006955.1:c.1798T>G | XP_016862444.1:p.Ser600Ala | |
NM_020754.4:c.2290T>G MANE Select | NP_065805.2:p.Ser764Ala |