Linked Data
ClinVar Variation Id:
409977
ClinVar RCV Id:
RCV000475694
dbSNP Id:
rs397514589
gnomAD v4:
1-2228870-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2228870C>G , CM000663.2:g.2228870C>G | GRCh38 |
| NC_000001.10:g.2160309C>G , CM000663.1:g.2160309C>G | GRCh37 |
| NC_000001.9:g.2150169C>G | NCBI36 |
| NG_013084.1:g.5176C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704337.1:n.137+1346C>G | ||
| ENST00000378536.5:c.104C>G MANE Select | ENSP00000367797.4:p.Pro35Arg | |
| ENST00000378536.4:c.104C>G | ENSP00000367797.4:p.Pro35Arg | |
| NM_003036.3:c.104C>G | NP_003027.1:p.Pro35Arg | |
| XM_005244775.2:c.104C>G | XP_005244832.1:p.Pro35Arg | |
| XM_005244775.3:c.104C>G | XP_005244832.1:p.Pro35Arg | |
| NM_003036.4:c.104C>G MANE Select | NP_003027.1:p.Pro35Arg |