HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133352511T>C , CM000671.2:g.133352511T>C | GRCh38 |
NC_000009.10:g.135209187T>C | NCBI36 |
NG_008477.1:g.8996A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.686A>G MANE Select | ENSP00000361042.3:p.Tyr229Cys | |
ENST00000371974.7:c.686A>G | ENSP00000361042.3:p.Tyr229Cys | |
ENST00000437995.1:n.596A>G | ||
ENST00000495952.5:n.676A>G | ||
ENST00000615505.4:c.359A>G | ENSP00000482067.1:p.Tyr120Cys | |
NM_001280787.1:c.359A>G | NP_001267716.1:p.Tyr120Cys | |
NM_003172.3:c.686A>G | NP_003163.1:p.Tyr229Cys | |
XM_011518942.1:c.359A>G | XP_011517244.1:p.Tyr120Cys | |
NM_003172.4:c.686A>G MANE Select | NP_003163.1:p.Tyr229Cys |