HGVS | Genome Assembly |
---|---|
NC_000019.10:g.50791799T>C , CM000681.2:g.50791799T>C | GRCh38 |
NC_000019.9:g.51295056T>C , CM000681.1:g.51295056T>C | GRCh37 |
NC_000019.8:g.55986868T>C | NCBI36 |
NG_052652.1:g.6385T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270593.2:c.447T>C (ACP4) MANE Select | ENSP00000270593.1:p.Asp149= | |
ENST00000636757.1:c.-60+606A>G (SMIM47) | ENSP00000489695.1:n.-60+606A>G | |
ENST00000270593.1:c.447T>C (ACP4) | ENSP00000270593.1:p.Asp149= | |
NM_033068.2:c.447T>C (ACP4) | NP_149059.1:p.Asp149= | |
XR_936026.1:n.424+606A>G | ||
XR_936026.2:n.434+606A>G | ||
NM_033068.3:c.447T>C (ACP4) MANE Select | NP_149059.1:p.Asp149= |