HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98186986A>C , CM000669.2:g.98186986A>C | GRCh38 |
NC_000007.13:g.97816298A>C , CM000669.1:g.97816298A>C | GRCh37 |
NC_000007.12:g.97654234A>C | NCBI36 |
NG_013375.1:g.85102A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297293.6:c.986A>C MANE Select | ENSP00000297293.5:p.Tyr329Ser | |
ENST00000297293.5:c.986A>C | ENSP00000297293.5:p.Tyr329Ser | |
NM_014916.3:c.986A>C | NP_055731.2:p.Tyr329Ser | |
XM_011515981.1:c.980A>C | XP_011514283.1:p.Tyr327Ser | |
XM_011515981.3:c.980A>C | XP_011514283.1:p.Tyr327Ser | |
NM_014916.4:c.986A>C MANE Select | NP_055731.2:p.Tyr329Ser |