HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31719241T>G , CM000668.2:g.31719241T>G | GRCh38 |
NC_000006.11:g.31687018T>G , CM000668.1:g.31687018T>G | GRCh37 |
NC_000006.10:g.31794997T>G | NCBI36 |
NG_029044.1:g.898T>G | |
NG_029044.2:g.898T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375819.3:c.233A>C (LY6G6C) MANE Select | ENSP00000364978.2:p.Gln78Pro | |
ENST00000375819.2:c.233A>C (LY6G6C) | ENSP00000364978.2:p.Gln78Pro | |
ENST00000460663.5:n.90+558T>G (MPIG6B) | ||
ENST00000495859.1:c.65A>C (LY6G6C) | ENSP00000433207.1:p.Gln22Pro | |
NM_025261.2:c.233A>C (LY6G6C) | NP_079537.1:p.Gln78Pro | |
NM_025261.3:c.233A>C (LY6G6C) MANE Select | NP_079537.1:p.Gln78Pro |