HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96145027C>A , CM000670.2:g.96145027C>A | GRCh38 |
NC_000008.10:g.97157255C>A , CM000670.1:g.97157255C>A | GRCh37 |
NC_000008.9:g.97226431C>A | NCBI36 |
NG_008981.1:g.20766G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287020.7:c.904G>T MANE Select | ENSP00000287020.4:p.Ala302Ser | |
ENST00000287020.6:c.904G>T | ENSP00000287020.4:p.Ala302Ser | |
ENST00000620978.1:c.793+49G>T | ENSP00000480170.1:n.793+49G>T | |
ENST00000621429.1:c.874+30G>T | ENSP00000483711.1:n.874+30G>T | |
NM_001001557.2:c.904G>T | NP_001001557.1:p.Ala302Ser | |
XM_011517030.1:c.505G>T | XP_011515332.1:p.Ala169Ser | |
NM_001001557.3:c.904G>T | NP_001001557.1:p.Ala302Ser | |
NM_001001557.4:c.904G>T MANE Select | NP_001001557.1:p.Ala302Ser |