HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734591G>A , CM000679.2:g.4734591G>A | GRCh38 |
NC_000017.10:g.4637886G>A , CM000679.1:g.4637886G>A | GRCh37 |
NC_000017.9:g.4584635G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*15C>T MANE Select | ENSP00000293778.7:n.*15C>T | |
ENST00000574412.6:c.*15C>T | ENSP00000459592.2:n.*15C>T | |
ENST00000293778.10:c.*15C>T | ENSP00000293778.6:n.*15C>T | |
ENST00000574412.5:c.*15C>T | ENSP00000459592.1:n.*15C>T | |
ENST00000575168.1:n.611C>T | ||
ENST00000576153.5:n.571C>T | ||
NM_001100812.1:c.*15C>T | NP_001094282.1:n.*15C>T | |
NM_022059.3:c.*15C>T | NP_071342.2:n.*15C>T | |
NM_022059.4:c.*15C>T | NP_071342.2:n.*15C>T | |
NM_001100812.2:c.*15C>T | NP_001094282.2:n.*15C>T | |
NM_001386809.1:c.*15C>T MANE Select | NP_001373738.1:n.*15C>T |