Linked Data
ClinVar Variation Id:
927581
ClinVar RCV Id:
RCV002375107
dbSNP Id:
rs1302665094
gnomAD v2:
2-21229922-A-G
gnomAD v3:
2-21007050-A-G
gnomAD v4:
2-21007050-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21007050A>G , CM000664.2:g.21007050A>G | GRCh38 |
| NC_000002.11:g.21229922A>G , CM000664.1:g.21229922A>G | GRCh37 |
| NC_000002.10:g.21083427A>G | NCBI36 |
| NG_011793.1:g.42024T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.9818T>C MANE Select | ENSP00000233242.1:p.Val3273Ala | |
| ENST00000616098.4:c.9818T>C | ENSP00000477990.1:p.Val3273Ala | |
| NM_000384.2:c.9818T>C | NP_000375.2:p.Val3273Ala | |
| XM_011532809.1:c.5869+3683T>C | XP_011531111.1:n.5869+3683T>C | |
| NM_000384.3:c.9818T>C MANE Select | NP_000375.3:p.Val3273Ala |