HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31719134T>A , CM000668.2:g.31719134T>A | GRCh38 |
NC_000006.11:g.31686911T>A , CM000668.1:g.31686911T>A | GRCh37 |
NC_000006.10:g.31794890T>A | NCBI36 |
NG_029044.1:g.791T>A | |
NG_029044.2:g.791T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375819.3:c.340A>T (LY6G6C) MANE Select | ENSP00000364978.2:p.Thr114Ser | |
ENST00000375819.2:c.340A>T (LY6G6C) | ENSP00000364978.2:p.Thr114Ser | |
ENST00000460663.5:n.90+451T>A (MPIG6B) | ||
ENST00000495859.1:c.172A>T (LY6G6C) | ENSP00000433207.1:p.Thr58Ser | |
NM_025261.2:c.340A>T (LY6G6C) | NP_079537.1:p.Thr114Ser | |
NM_025261.3:c.340A>T (LY6G6C) MANE Select | NP_079537.1:p.Thr114Ser |