HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45766465T>C , CM000681.2:g.45766465T>C | GRCh38 |
NC_000019.9:g.46269723T>C , CM000681.1:g.46269723T>C | GRCh37 |
NC_000019.8:g.50961563T>C | NCBI36 |
NG_012745.1:g.7775A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000317578.7:c.1494A>G MANE Select | ENSP00000316842.4:p.Ala498= | |
ENST00000317578.6:c.1494A>G | ENSP00000316842.4:p.Ala498= | |
ENST00000560160.1:c.587-354A>G | ||
ENST00000560168.1:c.*682A>G | ENSP00000453189.2:n.*682A>G | |
ENST00000622857.1:c.16-503A>G | ENSP00000481365.1:n.16-503A>G | |
NM_175875.4:c.1494A>G | NP_787071.2:p.Ala498= | |
NM_175875.5:c.1494A>G MANE Select | NP_787071.3:p.Ala498= |