Linked Data
ClinVar Variation Id:
2889780
ClinVar RCV Id:
RCV003720175
dbSNP Id:
rs1251510708
gnomAD v2:
13-110844646-A-C
gnomAD v4:
13-110192299-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110192299A>C , CM000675.2:g.110192299A>C | GRCh38 |
| NC_000013.10:g.110844646A>C , CM000675.1:g.110844646A>C | GRCh37 |
| NC_000013.9:g.109642647A>C | NCBI36 |
| NG_011544.2:g.119851T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.1466-15T>G MANE Select | ENSP00000364979.4:n.1466-15T>G | |
| ENST00000543140.6:c.1466-15T>G | ENSP00000443348.1:n.1466-15T>G | |
| ENST00000649738.1:n.1596-15T>G | ||
| ENST00000375820.8:c.1466-15T>G | ENSP00000364979.4:n.1466-15T>G | |
| ENST00000543140.5:c.1466-15T>G | ENSP00000443348.1:n.1466-15T>G | |
| NM_001303110.1:c.1466-15T>G | NP_001290039.1:n.1466-15T>G | |
| NM_001845.5:c.1466-15T>G | NP_001836.3:n.1466-15T>G | |
| XM_011521048.1:c.1274-15T>G | XP_011519350.1:n.1274-15T>G | |
| XM_011521048.2:c.1274-15T>G | XP_011519350.1:n.1274-15T>G | |
| NM_001845.6:c.1466-15T>G MANE Select | NP_001836.3:n.1466-15T>G | |
| NM_001303110.2:c.1466-15T>G | NP_001290039.1:n.1466-15T>G |