Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.50791774T>G , CM000681.2:g.50791774T>G | GRCh38 |
| NC_000019.9:g.51295031T>G , CM000681.1:g.51295031T>G | GRCh37 |
| NC_000019.8:g.55986843T>G | NCBI36 |
| NG_052652.1:g.6360T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270593.2:c.422T>G (ACP4) MANE Select | ENSP00000270593.1:p.Val141Gly | |
| ENST00000636757.1:c.-60+631A>C (SMIM47) | ENSP00000489695.1:n.-60+631A>C | |
| ENST00000270593.1:c.422T>G (ACP4) | ENSP00000270593.1:p.Val141Gly | |
| NM_033068.2:c.422T>G (ACP4) | NP_149059.1:p.Val141Gly | |
| XR_936026.1:n.424+631A>C | ||
| XR_936026.2:n.434+631A>C | ||
| NM_033068.3:c.422T>G (ACP4) MANE Select | NP_149059.1:p.Val141Gly |