Linked Data
ClinVar Variation Id:
56003
ClinVar RCV Id:
RCV000049412
dbSNP Id:
rs386833484
PubMed:
PMID:22779076
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107791093C>G , CM000669.2:g.107791093C>G | GRCh38 |
| NC_000007.13:g.107431538C>G , CM000669.1:g.107431538C>G | GRCh37 |
| NC_000007.12:g.107218774C>G | NCBI36 |
| NG_008046.1:g.17141G>C , LRG_683:g.17141G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340010.10:c.525G>C MANE Select | ENSP00000345873.5:p.Arg175Ser | |
| ENST00000340010.9:c.525G>C | ENSP00000345873.5:p.Arg175Ser | |
| ENST00000379083.7:c.*316G>C | ENSP00000368375.3:n.*316G>C | |
| NM_000111.2:c.525G>C , LRG_683t1:c.525G>C | NP_000102.1:p.Arg175Ser | |
| XM_011515867.1:c.525G>C | XP_011514169.1:p.Arg175Ser | |
| NM_000111.3:c.525G>C MANE Select | NP_000102.1:p.Arg175Ser |