HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96145081A>C , CM000670.2:g.96145081A>C | GRCh38 |
NC_000008.10:g.97157309A>C , CM000670.1:g.97157309A>C | GRCh37 |
NC_000008.9:g.97226485A>C | NCBI36 |
NG_008981.1:g.20712T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287020.7:c.850T>G MANE Select | ENSP00000287020.4:p.Ser284Ala | |
ENST00000287020.6:c.850T>G | ENSP00000287020.4:p.Ser284Ala | |
ENST00000620978.1:c.788T>G | ENSP00000480170.1:p.Ile263Ser | |
ENST00000621429.1:c.850T>G | ENSP00000483711.1:p.Ser284Ala | |
NM_001001557.2:c.850T>G | NP_001001557.1:p.Ser284Ala | |
XM_011517030.1:c.451T>G | XP_011515332.1:p.Ser151Ala | |
NM_001001557.3:c.850T>G | NP_001001557.1:p.Ser284Ala | |
NM_001001557.4:c.850T>G MANE Select | NP_001001557.1:p.Ser284Ala |