HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186544404T>A , CM000666.2:g.186544404T>A | GRCh38 |
NC_000004.11:g.187465558T>A , CM000666.1:g.187465558T>A | GRCh37 |
NC_000004.10:g.187702552T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703170.1:c.185-9847A>T | ENSP00000515216.1:n.185-9847A>T | |
ENST00000307161.5:c.185-9847A>T MANE Select | ENSP00000302811.5:n.185-9847A>T | |
ENST00000509111.2:c.147+10778A>T | ||
NM_005958.3:c.185-9847A>T | NP_005949.1:n.185-9847A>T | |
XR_939589.1:n.1982-1240T>A | ||
XR_939590.1:n.162-1240T>A | ||
NM_005958.4:c.185-9847A>T MANE Select | NP_005949.1:n.185-9847A>T | |
XR_939589.2:n.1982-1240T>A | ||
XR_939590.2:n.162-1240T>A |