HGVS | Genome Assembly |
---|---|
NC_000001.11:g.45508847C>T , CM000663.2:g.45508847C>T | GRCh38 |
NC_000001.10:g.45974519C>T , CM000663.1:g.45974519C>T | GRCh37 |
NC_000001.9:g.45747106C>T | NCBI36 |
NG_013378.1:g.13664C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401061.9:c.481C>T MANE Select | ENSP00000383840.4:p.Arg161Ter | |
ENST00000401061.8:c.481C>T | ENSP00000383840.4:p.Arg161Ter | |
ENST00000616135.1:c.310C>T | ENSP00000478859.1:p.Arg104Ter | |
NM_015506.2:c.481C>T | NP_056321.2:p.Arg161Ter | |
XM_005270724.3:c.286C>T | XP_005270781.1:p.Arg96Ter | |
XM_011541204.1:c.310C>T | XP_011539506.1:p.Arg104Ter | |
NM_001330540.1:c.310C>T | NP_001317469.1:p.Arg104Ter | |
XM_005270724.5:c.286C>T | XP_005270781.1:p.Arg96Ter | |
NM_015506.3:c.481C>T MANE Select | NP_056321.2:p.Arg161Ter | |
NM_001330540.2:c.310C>T | NP_001317469.1:p.Arg104Ter |