Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924270G>C , CM000675.2:g.27924270G>C | GRCh38 |
| NC_000013.10:g.28498407G>C , CM000675.1:g.28498407G>C | GRCh37 |
| NC_000013.9:g.27396407G>C | NCBI36 |
| NG_008183.1:g.9240G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.421G>C MANE Select | ENSP00000370421.4:p.Ala141Pro | |
| ENST00000381033.4:c.421G>C | ENSP00000370421.4:p.Ala141Pro | |
| NM_000209.3:c.421G>C | NP_000200.1:p.Ala141Pro | |
| XR_941578.1:n.3548G>C | ||
| XR_941579.1:n.2147G>C | ||
| XR_941580.1:n.1063G>C | ||
| XR_941578.2:n.3560G>C | ||
| XR_941580.2:n.1075G>C | ||
| NM_000209.4:c.421G>C MANE Select | NP_000200.1:p.Ala141Pro |