HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96145105C>A , CM000670.2:g.96145105C>A | GRCh38 |
NC_000008.10:g.97157333C>A , CM000670.1:g.97157333C>A | GRCh37 |
NC_000008.9:g.97226509C>A | NCBI36 |
NG_008981.1:g.20688G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287020.7:c.826G>T MANE Select | ENSP00000287020.4:p.Ala276Ser | |
ENST00000287020.6:c.826G>T | ENSP00000287020.4:p.Ala276Ser | |
ENST00000620978.1:c.764G>T | ENSP00000480170.1:p.Gly255Val | |
ENST00000621429.1:c.826G>T | ENSP00000483711.1:p.Ala276Ser | |
NM_001001557.2:c.826G>T | NP_001001557.1:p.Ala276Ser | |
XM_011517030.1:c.427G>T | XP_011515332.1:p.Ala143Ser | |
NM_001001557.3:c.826G>T | NP_001001557.1:p.Ala276Ser | |
NM_001001557.4:c.826G>T MANE Select | NP_001001557.1:p.Ala276Ser |