Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7529192A>C , CM000681.2:g.7529192A>C | GRCh38 |
| NC_000019.9:g.7594078A>C , CM000681.1:g.7594078A>C | GRCh37 |
| NC_000019.8:g.7500078A>C | NCBI36 |
| NG_013374.1:g.41A>C | |
| NG_015806.1:g.11583A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.1226A>C MANE Select | ENSP00000264079.5:p.His409Pro | |
| ENST00000264079.10:c.1226A>C | ENSP00000264079.5:p.His409Pro | |
| ENST00000394321.9:n.1541A>C | ||
| ENST00000594692.1:n.222A>C | ||
| ENST00000595860.5:n.409A>C | ||
| ENST00000599334.1:c.103A>C | ||
| NM_020533.2:c.1226A>C | NP_065394.1:p.His409Pro | |
| NM_020533.3:c.1226A>C MANE Select | NP_065394.1:p.His409Pro |