HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10656477G>A , CM000682.2:g.10656477G>A | GRCh38 |
NC_000020.10:g.10637125G>A , CM000682.1:g.10637125G>A | GRCh37 |
NC_000020.9:g.10585125G>A | NCBI36 |
NG_007496.1:g.22570C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.695-19C>T MANE Select | ENSP00000254958.4:n.695-19C>T | |
ENST00000254958.9:c.695-19C>T | ENSP00000254958.4:n.695-19C>T | |
ENST00000423891.6:n.561-19C>T | ||
NM_000214.2:c.695-19C>T | NP_000205.1:n.695-19C>T | |
NM_000214.3:c.695-19C>T MANE Select | NP_000205.1:n.695-19C>T |