HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56041923T>A , CM000674.2:g.56041923T>A | GRCh38 |
NC_000012.11:g.56435707T>A , CM000674.1:g.56435707T>A | GRCh37 |
NC_000012.10:g.54721974T>A | NCBI36 |
NG_023201.1:g.5022T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356464.10:c.-244T>A | ENSP00000348849.5:n.-244T>A | |
ENST00000646449.2:c.-244T>A MANE Select | ENSP00000496643.1:n.-244T>A | |
ENST00000356464.9:c.-244T>A | ENSP00000348849.5:n.-244T>A | |
ENST00000552361.1:c.-176T>A | ENSP00000450339.1:n.-176T>A | |
NM_001029.3:c.-244T>A | NP_001020.2:n.-244T>A | |
NM_001029.5:c.-244T>A MANE Select | NP_001020.2:n.-244T>A | |
XR_944989.3:n.81A>T | ||
XR_944990.3:n.81A>T |