Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818836C>G , CM000671.2:g.129818836C>G | GRCh38 |
| NC_000009.11:g.132581115C>G , CM000671.1:g.132581115C>G | GRCh37 |
| NC_000009.10:g.131620936C>G | NCBI36 |
| NG_008049.1:g.10327G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.529G>C MANE Select | ENSP00000345719.4:p.Ala177Pro | |
| ENST00000651202.1:c.625G>C | ENSP00000498222.1:p.Ala209Pro | |
| ENST00000351698.4:c.529G>C | ENSP00000345719.4:p.Ala177Pro | |
| ENST00000473604.2:n.639G>C | ||
| NM_000113.2:c.529G>C | NP_000104.1:p.Ala177Pro | |
| XR_929731.1:n.689G>C | ||
| XR_929731.3:n.557G>C | ||
| NM_000113.3:c.529G>C MANE Select | NP_000104.1:p.Ala177Pro |