Linked Data
dbSNP Id:
rs1422741271
gnomAD v2:
14-65542265-G-C
gnomAD v3:
14-65075547-G-C
gnomAD v4:
14-65075547-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65075547G>C , CM000676.2:g.65075547G>C | GRCh38 |
| NC_000014.8:g.65542265G>C , CM000676.1:g.65542265G>C | GRCh37 |
| NC_000014.7:g.64612018G>C | NCBI36 |
| NG_029830.1:g.31963C>G , LRG_530:g.31963C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000556892.6:c.*929C>G | ENSP00000452206.2:n.*929C>G | |
| ENST00000556979.6:c.*1865C>G | ENSP00000452378.1:n.*1865C>G | |
| ENST00000358664.9:c.*929C>G MANE Select | ENSP00000351490.4:n.*929C>G | |
| ENST00000651648.1:c.145-5178C>G | ENSP00000498863.1:n.145-5178C>G | |
| ENST00000284165.10:c.*2256C>G | ENSP00000284165.6:n.*2256C>G | |
| ENST00000341653.6:c.171+18161C>G | ENSP00000342482.2:n.171+18161C>G | |
| ENST00000358402.8:c.*929C>G | ENSP00000351175.4:n.*929C>G | |
| ENST00000358664.8:c.*929C>G | ENSP00000351490.4:n.*929C>G | |
| ENST00000394606.6:c.*1185C>G | ENSP00000378104.2:n.*1185C>G | |
| ENST00000555932.5:c.*904C>G | ENSP00000450763.1:n.*904C>G | |
| ENST00000618858.4:c.*1201C>G | ENSP00000480127.1:n.*1201C>G | |
| NM_001271069.1:c.144+18161C>G | NP_001257998.1:n.144+18161C>G | |
| NM_002382.4:c.*929C>G | NP_002373.3:n.*929C>G | |
| NM_145112.2:c.*929C>G | NP_660087.1:n.*929C>G | |
| NM_145113.2:c.*1201C>G | NP_660088.1:n.*1201C>G | |
| NM_197957.3:c.171+18161C>G | NP_932061.1:n.171+18161C>G | |
| NR_073137.1:n.1536C>G | ||
| XR_429315.2:n.1699C>G | ||
| NM_001320415.1:c.*929C>G | NP_001307344.1:n.*929C>G | |
| XM_017021312.2:c.*929C>G | XP_016876801.1:n.*929C>G | |
| XM_017021313.1:c.*929C>G | XP_016876802.1:n.*929C>G | |
| XR_001750326.2:n.1757C>G | ||
| XR_001750327.2:n.1676C>G | ||
| XR_002957553.1:n.2190C>G | ||
| XR_943450.3:n.1780C>G | ||
| XR_943451.3:n.1796C>G | ||
| XR_943452.3:n.1741C>G | ||
| NM_001320415.2:c.*929C>G | NP_001307344.1:n.*929C>G | |
| NM_002382.5:c.*929C>G MANE Select | NP_002373.3:n.*929C>G | |
| NM_145112.3:c.*929C>G | NP_660087.1:n.*929C>G | |
| NM_145113.3:c.*1201C>G | NP_660088.1:n.*1201C>G | |
| NM_001271069.2:c.144+18161C>G | NP_001257998.1:n.144+18161C>G | |
| NM_197957.4:c.171+18161C>G | NP_932061.1:n.171+18161C>G |