HGVS | Genome Assembly |
---|---|
NC_000019.10:g.50791795A>T , CM000681.2:g.50791795A>T | GRCh38 |
NC_000019.9:g.51295052A>T , CM000681.1:g.51295052A>T | GRCh37 |
NC_000019.8:g.55986864A>T | NCBI36 |
NG_052652.1:g.6381A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270593.2:c.443A>T (ACP4) MANE Select | ENSP00000270593.1:p.Glu148Val | |
ENST00000636757.1:c.-60+610T>A (SMIM47) | ENSP00000489695.1:n.-60+610T>A | |
ENST00000270593.1:c.443A>T (ACP4) | ENSP00000270593.1:p.Glu148Val | |
NM_033068.2:c.443A>T (ACP4) | NP_149059.1:p.Glu148Val | |
XR_936026.1:n.424+610T>A | ||
XR_936026.2:n.434+610T>A | ||
NM_033068.3:c.443A>T (ACP4) MANE Select | NP_149059.1:p.Glu148Val |