Linked Data
ClinVar Variation Id:
354021
dbSNP Id:
rs143356896
ExAC:
5:60224682 T / C
gnomAD v2:
5-60224682-T-C
gnomAD v3:
5-60928855-T-C
gnomAD v4:
5-60928855-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.60928855T>C , CM000667.2:g.60928855T>C | GRCh38 |
| NC_000005.9:g.60224682T>C , CM000667.1:g.60224682T>C | GRCh37 |
| NC_000005.8:g.60260439T>C | NCBI36 |
| NG_009289.1:g.21224A>G , LRG_466:g.21224A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439176.6:c.173+9A>G | ENSP00000408344.2:n.173+9A>G | |
| ENST00000647431.2:c.173+9A>G | ENSP00000494726.2:n.173+9A>G | |
| ENST00000647486.2:c.173+9A>G | ENSP00000494466.2:n.173+9A>G | |
| ENST00000675042.2:c.-2+9A>G | ENSP00000502082.2:n.-2+9A>G | |
| ENST00000675452.2:c.173+9A>G | ENSP00000506954.1:n.173+9A>G | |
| ENST00000682041.1:n.232A>G | ||
| ENST00000682217.1:c.173+9A>G | ENSP00000507570.1:n.173+9A>G | |
| ENST00000682246.1:n.229+9A>G | ||
| ENST00000682375.1:c.-2+9A>G | ENSP00000507551.1:n.-2+9A>G | |
| ENST00000682380.1:n.229+9A>G | ||
| ENST00000682418.1:n.229+9A>G | ||
| ENST00000682874.1:n.223+9A>G | ||
| ENST00000683052.1:c.78-10467A>G | ENSP00000507072.1:n.78-10467A>G | |
| ENST00000683199.1:n.195+9A>G | ||
| ENST00000683460.1:c.173+9A>G | ENSP00000507820.1:n.173+9A>G | |
| ENST00000684394.1:n.228+9A>G | ||
| ENST00000684453.1:n.223+9A>G | ||
| ENST00000684621.1:n.229+9A>G | ||
| ENST00000265038.10:c.173+9A>G | ENSP00000265038.6:n.173+9A>G | |
| ENST00000497892.6:c.173+9A>G | ENSP00000501805.1:n.173+9A>G | |
| ENST00000643034.1:c.173+9A>G | ENSP00000496080.1:n.173+9A>G | |
| ENST00000643708.1:c.173+9A>G | ENSP00000494199.1:n.173+9A>G | |
| ENST00000647431.1:c.124+9A>G | ||
| ENST00000647486.1:c.124+9A>G | ||
| ENST00000675042.1:c.-2+9A>G | ENSP00000502082.1:n.-2+9A>G | |
| ENST00000675229.1:c.173+9A>G | ENSP00000502154.1:n.173+9A>G | |
| ENST00000675378.1:c.173+9A>G | ENSP00000502535.1:n.173+9A>G | |
| ENST00000675920.1:n.294+9A>G | ||
| ENST00000676185.1:c.173+9A>G MANE Select | ENSP00000501614.1:n.173+9A>G | |
| ENST00000265038.9:c.173+9A>G | ENSP00000265038.5:n.173+9A>G | |
| ENST00000381118.7:c.173+9A>G | ENSP00000370510.3:n.173+9A>G | |
| ENST00000439176.5:c.-2+9A>G | ENSP00000408344.1:n.-2+9A>G | |
| ENST00000477893.1:n.224+9A>G | ||
| ENST00000497892.5:n.216+9A>G | ||
| NM_000082.3:c.173+9A>G , LRG_466t1:c.173+9A>G | NP_000073.1:n.173+9A>G | |
| NM_001007233.2:c.-220+9A>G | NP_001007234.1:n.-220+9A>G | |
| NM_001007234.2:c.173+9A>G | NP_001007235.1:n.173+9A>G | |
| NM_001290285.1:c.-205+9A>G | NP_001277214.1:n.-205+9A>G | |
| NM_001007234.3:c.173+9A>G | NP_001007235.1:n.173+9A>G | |
| NM_000082.4:c.173+9A>G MANE Select | NP_000073.1:n.173+9A>G | |
| NM_001007233.3:c.-220+9A>G | NP_001007234.1:n.-220+9A>G | |
| NM_001290285.2:c.-205+9A>G | NP_001277214.1:n.-205+9A>G |