HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110602171T>A , CM000672.2:g.110602171T>A | GRCh38 |
NC_000010.10:g.112361929T>A , CM000672.1:g.112361929T>A | GRCh37 |
NC_000010.9:g.112351919T>A | NCBI36 |
NG_012217.1:g.39481T>A , LRG_774:g.39481T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.5331T>A | ||
ENST00000685743.1:n.2806T>A | ||
ENST00000686057.1:n.1449T>A | ||
ENST00000689321.1:n.2061T>A | ||
ENST00000689986.1:n.887T>A | ||
ENST00000361804.5:c.3098T>A MANE Select | ENSP00000354720.5:p.Phe1033Tyr | |
ENST00000361804.4:c.3098T>A | ENSP00000354720.4:p.Phe1033Tyr | |
NM_005445.3:c.3098T>A , LRG_774t1:c.3098T>A | NP_005436.1:p.Phe1033Tyr | |
NM_005445.4:c.3098T>A MANE Select | NP_005436.1:p.Phe1033Tyr |