HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33075601A>T , CM000668.2:g.33075601A>T | GRCh38 |
NC_000006.11:g.33043378A>T , CM000668.1:g.33043378A>T | GRCh37 |
NC_000006.10:g.33151356A>T | NCBI36 |
NG_033241.1:g.10178T>A | |
NG_033242.1:g.4676A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000417724.1:c.-140-1891T>A | ENSP00000398134.1:n.-140-1891T>A | |
ENST00000419277.5:c.-99-1932T>A | ENSP00000393566.1:n.-99-1932T>A | |
ENST00000453337.1:c.-202-1829T>A | ENSP00000390929.1:n.-202-1829T>A | |
ENST00000476642.5:n.76+5079T>A | ||
NM_001242524.1:c.-99-1932T>A | NP_001229453.1:n.-99-1932T>A | |
NM_001242525.1:c.-23-2008T>A | NP_001229454.1:n.-23-2008T>A | |
NM_001242524.2:c.-99-1932T>A | NP_001229453.1:n.-99-1932T>A | |
NM_001242525.2:c.-23-2008T>A | NP_001229454.1:n.-23-2008T>A |