HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150851888T>C , CM000669.2:g.150851888T>C | GRCh38 |
NC_000007.13:g.150548976T>C , CM000669.1:g.150548976T>C | GRCh37 |
NC_000007.12:g.150179909T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000467291.5:c.-92-227T>C | ENSP00000418328.1:n.-92-227T>C | |
ENST00000493429.5:c.-92-227T>C | ENSP00000418614.1:n.-92-227T>C | |
XM_011516008.1:c.-181-227T>C | XP_011514310.1:n.-181-227T>C | |
XM_011516009.1:c.-92-227T>C | XP_011514311.1:n.-92-227T>C | |
XR_928169.1:n.296-10443A>G | ||
XR_928170.1:n.426-10443A>G | ||
XR_928171.1:n.298-10443A>G | ||
XM_017011944.1:c.-92-227T>C | XP_016867433.1:n.-92-227T>C | |
XM_017011945.1:c.-92-227T>C | XP_016867434.1:n.-92-227T>C | |
XR_928169.2:n.302-10443A>G | ||
XR_928171.2:n.302-10443A>G |