Linked Data
ClinVar Variation Id:
1797779
ClinVar RCV Id:
RCV002440029
dbSNP Id:
rs1392259151
gnomAD v3:
21-34370770-A-C
gnomAD v4:
21-34370770-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370770A>C , CM000683.2:g.34370770A>C | GRCh38 |
| NC_000021.8:g.35743069A>C , CM000683.1:g.35743069A>C | GRCh37 |
| NC_000021.7:g.34664939A>C | NCBI36 |
| NG_008804.1:g.11747A>C , LRG_291:g.11747A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290310.4:c.292A>C MANE Select | ENSP00000290310.2:p.Ser98Arg | |
| ENST00000290310.3:c.292A>C | ENSP00000290310.2:p.Ser98Arg | |
| NM_172201.1:c.292A>C , LRG_291t1:c.292A>C | NP_751951.1:p.Ser98Arg | |
| XR_937683.1:n.551T>G | ||
| XR_937684.1:n.551T>G | ||
| XR_001755012.2:n.672T>G | ||
| XR_001755013.2:n.551T>G | ||
| XR_937683.2:n.551T>G | ||
| NM_172201.2:c.292A>C MANE Select | NP_751951.1:p.Ser98Arg |