HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150846495T>A , CM000669.2:g.150846495T>A | GRCh38 |
NC_000007.13:g.150543583T>A , CM000669.1:g.150543583T>A | GRCh37 |
NC_000007.12:g.150174516T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000467291.5:c.-92-5620T>A | ENSP00000418328.1:n.-92-5620T>A | |
ENST00000493429.5:c.-92-5620T>A | ENSP00000418614.1:n.-92-5620T>A | |
XM_011516008.1:c.-181-5620T>A | XP_011514310.1:n.-181-5620T>A | |
XM_011516009.1:c.-92-5620T>A | XP_011514311.1:n.-92-5620T>A | |
XR_928169.1:n.296-5050A>T | ||
XR_928170.1:n.426-5050A>T | ||
XR_928171.1:n.298-5050A>T | ||
XM_017011944.1:c.-92-5620T>A | XP_016867433.1:n.-92-5620T>A | |
XM_017011945.1:c.-92-5620T>A | XP_016867434.1:n.-92-5620T>A | |
XR_928169.2:n.302-5050A>T | ||
XR_928171.2:n.302-5050A>T |