Linked Data
ClinVar Variation Id:
2963898
ClinVar RCV Id:
RCV003825536
dbSNP Id:
rs776270218
gnomAD v2:
15-73615231-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322890C>G , CM000677.2:g.73322890C>G | GRCh38 |
| NC_000015.9:g.73615231C>G , CM000677.1:g.73615231C>G | GRCh37 |
| NC_000015.8:g.71402284C>G | NCBI36 |
| NG_009063.1:g.51375G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3203G>C MANE Select | ENSP00000261917.3:p.Arg1068Pro | |
| ENST00000261917.3:c.3203G>C | ENSP00000261917.3:p.Arg1068Pro | |
| NM_005477.2:c.3203G>C | NP_005468.1:p.Arg1068Pro | |
| XM_011521148.1:c.1985G>C | XP_011519450.1:p.Arg662Pro | |
| XM_011521148.2:c.1985G>C | XP_011519450.1:p.Arg662Pro | |
| NM_005477.3:c.3203G>C MANE Select | NP_005468.1:p.Arg1068Pro |