Linked Data
dbSNP Id:
rs1029534413
gnomAD v2:
14-65544825-T-C
gnomAD v3:
14-65078107-T-C
gnomAD v4:
14-65078107-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.65078107T>C , CM000676.2:g.65078107T>C | GRCh38 |
| NC_000014.8:g.65544825T>C , CM000676.1:g.65544825T>C | GRCh37 |
| NC_000014.7:g.64614578T>C | NCBI36 |
| NG_029830.1:g.29403A>G , LRG_530:g.29403A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000556892.6:c.-48-71A>G | ENSP00000452206.2:n.-48-71A>G | |
| ENST00000556979.6:c.172-71A>G | ENSP00000452378.1:n.172-71A>G | |
| ENST00000358664.9:c.172-71A>G MANE Select | ENSP00000351490.4:n.172-71A>G | |
| ENST00000651648.1:c.145-7738A>G | ENSP00000498863.1:n.145-7738A>G | |
| ENST00000284165.10:c.172-71A>G | ENSP00000284165.6:n.172-71A>G | |
| ENST00000341653.6:c.171+15601A>G | ENSP00000342482.2:n.171+15601A>G | |
| ENST00000358402.8:c.145-71A>G | ENSP00000351175.4:n.145-71A>G | |
| ENST00000358664.8:c.172-71A>G | ENSP00000351490.4:n.172-71A>G | |
| ENST00000394606.6:c.172-71A>G | ENSP00000378104.2:n.172-71A>G | |
| ENST00000553928.5:c.172-71A>G | ENSP00000451907.1:n.172-71A>G | |
| ENST00000553951.1:n.249-71A>G | ||
| ENST00000555419.5:c.64-71A>G | ENSP00000452405.1:n.64-71A>G | |
| ENST00000555667.5:c.145-71A>G | ENSP00000452286.1:n.145-71A>G | |
| ENST00000555932.5:c.37-1444A>G | ENSP00000450763.1:n.37-1444A>G | |
| ENST00000556443.5:c.145-71A>G | ENSP00000450818.1:n.145-71A>G | |
| ENST00000556892.5:c.-48-71A>G | ENSP00000452206.1:n.-48-71A>G | |
| ENST00000556979.5:c.172-71A>G | ENSP00000452378.1:n.172-71A>G | |
| ENST00000557277.5:c.-103-71A>G | ENSP00000450955.1:n.-103-71A>G | |
| ENST00000557746.5:c.145-71A>G | ENSP00000452197.1:n.145-71A>G | |
| ENST00000618858.4:c.172-71A>G | ENSP00000480127.1:n.172-71A>G | |
| NM_001271069.1:c.144+15601A>G | NP_001257998.1:n.144+15601A>G | |
| NM_002382.4:c.172-71A>G | NP_002373.3:n.172-71A>G | |
| NM_145112.2:c.145-71A>G | NP_660087.1:n.145-71A>G | |
| NM_145113.2:c.172-71A>G | NP_660088.1:n.172-71A>G | |
| NM_197957.3:c.171+15601A>G | NP_932061.1:n.171+15601A>G | |
| NR_073137.1:n.296-71A>G | ||
| XM_011536773.1:c.172-71A>G | XP_011535075.1:n.172-71A>G | |
| XR_429315.2:n.374-71A>G | ||
| XR_943450.1:n.374-71A>G | ||
| XR_943451.1:n.374-71A>G | ||
| XR_943452.1:n.336-71A>G | ||
| NM_001320415.1:c.-103-71A>G | NP_001307344.1:n.-103-71A>G | |
| XM_011536773.3:c.172-71A>G | XP_011535075.1:n.172-71A>G | |
| XM_017021312.2:c.-103-71A>G | XP_016876801.1:n.-103-71A>G | |
| XM_017021313.1:c.-103-71A>G | XP_016876802.1:n.-103-71A>G | |
| XR_001750326.2:n.335-71A>G | ||
| XR_001750327.2:n.335-71A>G | ||
| XR_002957553.1:n.365-71A>G | ||
| XR_943450.3:n.374-71A>G | ||
| XR_943451.3:n.374-71A>G | ||
| XR_943452.3:n.335-71A>G | ||
| NM_001320415.2:c.-103-71A>G | NP_001307344.1:n.-103-71A>G | |
| NM_002382.5:c.172-71A>G MANE Select | NP_002373.3:n.172-71A>G | |
| NM_145112.3:c.145-71A>G | NP_660087.1:n.145-71A>G | |
| NM_145113.3:c.172-71A>G | NP_660088.1:n.172-71A>G | |
| NM_001271069.2:c.144+15601A>G | NP_001257998.1:n.144+15601A>G | |
| NM_197957.4:c.171+15601A>G | NP_932061.1:n.171+15601A>G |