Linked Data
dbSNP Id:
rs899851478
gnomAD v2:
14-65542324-T-C
gnomAD v3:
14-65075606-T-C
gnomAD v4:
14-65075606-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65075606T>C , CM000676.2:g.65075606T>C | GRCh38 |
| NC_000014.8:g.65542324T>C , CM000676.1:g.65542324T>C | GRCh37 |
| NC_000014.7:g.64612077T>C | NCBI36 |
| NG_029830.1:g.31904A>G , LRG_530:g.31904A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000556892.6:c.*870A>G | ENSP00000452206.2:n.*870A>G | |
| ENST00000556979.6:c.*1806A>G | ENSP00000452378.1:n.*1806A>G | |
| ENST00000358664.9:c.*870A>G MANE Select | ENSP00000351490.4:n.*870A>G | |
| ENST00000651648.1:c.145-5237A>G | ENSP00000498863.1:n.145-5237A>G | |
| ENST00000284165.10:c.*2197A>G | ENSP00000284165.6:n.*2197A>G | |
| ENST00000341653.6:c.171+18102A>G | ENSP00000342482.2:n.171+18102A>G | |
| ENST00000358402.8:c.*870A>G | ENSP00000351175.4:n.*870A>G | |
| ENST00000358664.8:c.*870A>G | ENSP00000351490.4:n.*870A>G | |
| ENST00000394606.6:c.*1126A>G | ENSP00000378104.2:n.*1126A>G | |
| ENST00000555932.5:c.*845A>G | ENSP00000450763.1:n.*845A>G | |
| ENST00000618858.4:c.*1142A>G | ENSP00000480127.1:n.*1142A>G | |
| NM_001271069.1:c.144+18102A>G | NP_001257998.1:n.144+18102A>G | |
| NM_002382.4:c.*870A>G | NP_002373.3:n.*870A>G | |
| NM_145112.2:c.*870A>G | NP_660087.1:n.*870A>G | |
| NM_145113.2:c.*1142A>G | NP_660088.1:n.*1142A>G | |
| NM_197957.3:c.171+18102A>G | NP_932061.1:n.171+18102A>G | |
| NR_073137.1:n.1477A>G | ||
| XR_429315.2:n.1640A>G | ||
| NM_001320415.1:c.*870A>G | NP_001307344.1:n.*870A>G | |
| XM_017021312.2:c.*870A>G | XP_016876801.1:n.*870A>G | |
| XM_017021313.1:c.*870A>G | XP_016876802.1:n.*870A>G | |
| XR_001750326.2:n.1698A>G | ||
| XR_001750327.2:n.1617A>G | ||
| XR_002957553.1:n.2131A>G | ||
| XR_943450.3:n.1721A>G | ||
| XR_943451.3:n.1737A>G | ||
| XR_943452.3:n.1682A>G | ||
| NM_001320415.2:c.*870A>G | NP_001307344.1:n.*870A>G | |
| NM_002382.5:c.*870A>G MANE Select | NP_002373.3:n.*870A>G | |
| NM_145112.3:c.*870A>G | NP_660087.1:n.*870A>G | |
| NM_145113.3:c.*1142A>G | NP_660088.1:n.*1142A>G | |
| NM_001271069.2:c.144+18102A>G | NP_001257998.1:n.144+18102A>G | |
| NM_197957.4:c.171+18102A>G | NP_932061.1:n.171+18102A>G |