Linked Data
ClinVar Variation Id:
65885
dbSNP Id:
rs201346271
ExAC:
2:219677144 G / C
gnomAD v2:
2-219677144-G-C
gnomAD v3:
2-218812421-G-C
gnomAD v4:
2-218812421-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812421G>C , CM000664.2:g.218812421G>C | GRCh38 |
| NC_000002.11:g.219677144G>C , CM000664.1:g.219677144G>C | GRCh37 |
| NC_000002.10:g.219385388G>C | NCBI36 |
| NG_007959.1:g.35673G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000258415.9:c.646G>C MANE Select | ENSP00000258415.4:p.Ala216Pro | |
| ENST00000258415.8:c.646G>C | ENSP00000258415.4:p.Ala216Pro | |
| ENST00000411688.1:c.364G>C | ENSP00000392671.1:p.Ala122Pro | |
| ENST00000445971.1:c.*107G>C | ENSP00000404945.1:n.*107G>C | |
| ENST00000466602.1:n.464G>C | ||
| ENST00000494263.5:n.1080G>C | ||
| NM_000784.3:c.646G>C | NP_000775.1:p.Ala216Pro | |
| XM_017003488.2:c.226G>C | XP_016858977.1:p.Ala76Pro | |
| NM_000784.4:c.646G>C MANE Select | NP_000775.1:p.Ala216Pro |