HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8120710G>C , CM000679.2:g.8120710G>C | GRCh38 |
NC_000017.10:g.8024028G>C , CM000679.1:g.8024028G>C | GRCh37 |
NC_000017.9:g.7964753G>C | NCBI36 |
NG_015807.1:g.3207C>G | |
NG_015816.1:g.8383C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000541682.7:c.*861C>G MANE Select | ENSP00000446205.2:n.*861C>G | |
ENST00000541682.6:c.1554C>G | ENSP00000446205.2:n.1554C>G | |
NM_001165967.1:c.*861C>G | NP_001159439.1:n.*861C>G | |
NM_032580.3:c.*861C>G | NP_115969.2:n.*861C>G | |
XM_011524038.1:c.*861C>G | XP_011522340.1:n.*861C>G | |
XR_934203.1:n.69+896G>C | ||
XM_017025232.1:c.*861C>G | XP_016880721.1:n.*861C>G | |
XM_024451007.1:c.*861C>G | XP_024306775.1:n.*861C>G | |
NM_001165967.2:c.*861C>G MANE Select | NP_001159439.1:n.*861C>G | |
NM_032580.4:c.*861C>G | NP_115969.2:n.*861C>G |