HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31719239T>C , CM000668.2:g.31719239T>C | GRCh38 |
NC_000006.11:g.31687016T>C , CM000668.1:g.31687016T>C | GRCh37 |
NC_000006.10:g.31794995T>C | NCBI36 |
NG_029044.1:g.896T>C | |
NG_029044.2:g.896T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375819.3:c.235A>G (LY6G6C) MANE Select | ENSP00000364978.2:p.Thr79Ala | |
ENST00000375819.2:c.235A>G (LY6G6C) | ENSP00000364978.2:p.Thr79Ala | |
ENST00000460663.5:n.90+556T>C (MPIG6B) | ||
ENST00000495859.1:c.67A>G (LY6G6C) | ENSP00000433207.1:p.Thr23Ala | |
NM_025261.2:c.235A>G (LY6G6C) | NP_079537.1:p.Thr79Ala | |
NM_025261.3:c.235A>G (LY6G6C) MANE Select | NP_079537.1:p.Thr79Ala |