HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133353887A>C , CM000671.2:g.133353887A>C | GRCh38 |
NC_000009.10:g.135210563A>C | NCBI36 |
NG_008477.1:g.7620T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371974.8:c.377T>G MANE Select | ENSP00000361042.3:p.Phe126Cys | |
ENST00000371974.7:c.377T>G | ENSP00000361042.3:p.Phe126Cys | |
ENST00000437995.1:n.323T>G | ||
ENST00000495952.5:n.367T>G | ||
ENST00000615505.4:c.50T>G | ENSP00000482067.1:p.Phe17Cys | |
NM_001280787.1:c.50T>G | NP_001267716.1:p.Phe17Cys | |
NM_003172.3:c.377T>G | NP_003163.1:p.Phe126Cys | |
XM_011518942.1:c.50T>G | XP_011517244.1:p.Phe17Cys | |
NM_003172.4:c.377T>G MANE Select | NP_003163.1:p.Phe126Cys |