HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10643827C>A , CM000682.2:g.10643827C>A | GRCh38 |
NC_000020.10:g.10624475C>A , CM000682.1:g.10624475C>A | GRCh37 |
NC_000020.9:g.10572475C>A | NCBI36 |
NG_007496.1:g.35220G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.2409G>T MANE Select | ENSP00000254958.4:p.Trp803Cys | |
ENST00000617965.2:n.2998G>T | ||
ENST00000254958.9:c.2409G>T | ENSP00000254958.4:p.Trp803Cys | |
ENST00000423891.6:n.2275G>T | ||
NM_000214.2:c.2409G>T | NP_000205.1:p.Trp803Cys | |
NM_000214.3:c.2409G>T MANE Select | NP_000205.1:p.Trp803Cys |