Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134835131T>C , CM000671.2:g.134835131T>C | GRCh38 |
| NC_000009.11:g.137726977T>C , CM000671.1:g.137726977T>C | GRCh37 |
| NC_000009.10:g.136866798T>C | NCBI36 |
| NG_008030.1:g.198326T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.5297T>C | ENSP00000360885.4:p.Phe1766Ser | |
| ENST00000371817.8:c.5297T>C MANE Select | ENSP00000360882.3:p.Phe1766Ser | |
| ENST00000371817.7:c.5297T>C | ENSP00000360882.3:p.Phe1766Ser | |
| ENST00000371820.3:c.555T>C | ||
| ENST00000618395.4:c.5297T>C | ENSP00000481360.1:p.Phe1766Ser | |
| NM_000093.4:c.5297T>C | NP_000084.3:p.Phe1766Ser | |
| NM_001278074.1:c.5297T>C | NP_001265003.1:p.Phe1766Ser | |
| NR_103451.2:n.71-14922A>G | ||
| NM_000093.5:c.5297T>C MANE Select | NP_000084.3:p.Phe1766Ser |