HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764537A>C , CM000674.2:g.57764537A>C | GRCh38 |
NC_000012.11:g.58158320A>C , CM000674.1:g.58158320A>C | GRCh37 |
NC_000012.10:g.56444587A>C | NCBI36 |
NG_007076.1:g.7657T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000713544.1:c.1058T>G | ENSP00000518840.1:p.Leu353Arg | |
ENST00000713545.1:c.1035T>G | ENSP00000518841.1:p.Ala345= | |
ENST00000228606.9:c.977T>G MANE Select | ENSP00000228606.4:p.Leu326Arg | |
ENST00000228606.8:c.977T>G | ENSP00000228606.4:p.Leu326Arg | |
ENST00000546567.5:c.272T>G | ENSP00000449472.1:p.Leu91Arg | |
ENST00000547344.5:n.1116T>G | ||
NM_000785.3:c.977T>G | NP_000776.1:p.Leu326Arg | |
NM_000785.4:c.977T>G MANE Select | NP_000776.1:p.Leu326Arg |