HGVS | Genome Assembly |
---|---|
NC_000015.10:g.45103974G>C , CM000677.2:g.45103974G>C | GRCh38 |
NC_000015.9:g.45396172G>C , CM000677.1:g.45396172G>C | GRCh37 |
NC_000015.8:g.43183464G>C | NCBI36 |
NG_009447.1:g.15188C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389039.11:c.2640C>G MANE Select | ENSP00000373691.7:p.Phe880Leu | |
ENST00000389039.10:c.2640C>G | ENSP00000373691.6:p.Phe880Leu | |
ENST00000558383.1:n.4371C>G | ||
ENST00000603300.1:c.2640C>G | ENSP00000475084.1:p.Phe880Leu | |
NM_014080.4:c.2640C>G | NP_054799.4:p.Phe880Leu | |
XM_005254421.2:c.2640C>G | XP_005254478.1:p.Phe880Leu | |
NM_001363711.1:c.2640C>G | NP_001350640.1:p.Phe880Leu | |
NM_001363711.2:c.2640C>G MANE Select | NP_001350640.1:p.Phe880Leu | |
NM_014080.5:c.2640C>G | NP_054799.4:p.Phe880Leu |