HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110582034G>A , CM000672.2:g.110582034G>A | GRCh38 |
NC_000010.10:g.112341792G>A , CM000672.1:g.112341792G>A | GRCh37 |
NC_000010.9:g.112331782G>A | NCBI36 |
NG_012217.1:g.19344G>A , LRG_774:g.19344G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.792G>A | ||
ENST00000687823.1:n.573G>A | ||
ENST00000689932.1:n.2722G>A | ||
ENST00000691297.1:n.792G>A | ||
ENST00000691527.1:n.1462G>A | ||
ENST00000692792.1:n.778G>A | ||
ENST00000361804.5:c.659G>A MANE Select | ENSP00000354720.5:p.Arg220Lys | |
ENST00000361804.4:c.659G>A | ENSP00000354720.4:p.Arg220Lys | |
NM_005445.3:c.659G>A , LRG_774t1:c.659G>A | NP_005436.1:p.Arg220Lys | |
NM_005445.4:c.659G>A MANE Select | NP_005436.1:p.Arg220Lys |