Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67435999T>A , CM000678.2:g.67435999T>A | GRCh38 |
| NC_000016.9:g.67469902T>A , CM000678.1:g.67469902T>A | GRCh37 |
| NC_000016.8:g.66027403T>A | NCBI36 |
| NG_016549.1:g.9867T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326152.6:c.521T>A MANE Select | ENSP00000316786.5:p.Val174Asp | |
| ENST00000326152.5:c.521T>A | ENSP00000316786.5:p.Val174Asp | |
| ENST00000566606.1:c.499T>A | ENSP00000473429.1:n.499T>A | |
| ENST00000567684.2:n.384T>A | ||
| NM_000196.3:c.521T>A | NP_000187.3:p.Val174Asp | |
| NM_000196.4:c.521T>A MANE Select | NP_000187.3:p.Val174Asp |