Linked Data
dbSNP Id:
rs747514545
ExAC:
3:128628290 T / C
gnomAD v2:
3-128628290-T-C
gnomAD v4:
3-128909447-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128909447T>C , CM000665.2:g.128909447T>C | GRCh38 |
| NC_000003.11:g.128628290T>C , CM000665.1:g.128628290T>C | GRCh37 |
| NC_000003.10:g.130110980T>C | NCBI36 |
| NG_017064.1:g.34958T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308982.12:c.1563+26T>C MANE Select | ENSP00000312618.7:n.1563+26T>C | |
| ENST00000511325.2:n.1667T>C | ||
| ENST00000679399.1:c.*1734+26T>C | ENSP00000505434.1:n.*1734+26T>C | |
| ENST00000679431.1:c.*1439+26T>C | ENSP00000506440.1:n.*1439+26T>C | |
| ENST00000679613.1:c.1563+26T>C | ENSP00000504971.1:n.1563+26T>C | |
| ENST00000679715.1:c.1194+26T>C | ENSP00000506228.1:n.1194+26T>C | |
| ENST00000679824.1:c.*2869+26T>C | ENSP00000505516.1:n.*2869+26T>C | |
| ENST00000679990.1:n.1824T>C | ||
| ENST00000680636.1:c.1563+26T>C | ENSP00000504886.1:n.1563+26T>C | |
| ENST00000680638.1:n.1342T>C | ||
| ENST00000680744.1:c.*916+26T>C | ENSP00000505243.1:n.*916+26T>C | |
| ENST00000680764.1:c.*2967+26T>C | ENSP00000505126.1:n.*2967+26T>C | |
| ENST00000681319.1:n.2349+26T>C | ||
| ENST00000681367.1:c.1563+26T>C | ENSP00000505309.1:n.1563+26T>C | |
| ENST00000681552.1:c.1150-3060T>C | ENSP00000505699.1:n.1150-3060T>C | |
| ENST00000681583.1:c.1563+26T>C | ENSP00000506340.1:n.1563+26T>C | |
| ENST00000681585.1:c.*182+26T>C | ENSP00000506316.1:n.*182+26T>C | |
| ENST00000681784.1:n.1667T>C | ||
| ENST00000681886.1:c.*782T>C | ENSP00000506500.1:n.*782T>C | |
| ENST00000308982.11:c.1563+26T>C | ENSP00000312618.7:n.1563+26T>C | |
| ENST00000505867.5:c.*1363+26T>C | ENSP00000425346.1:n.*1363+26T>C | |
| ENST00000508971.1:c.852+26T>C | ENSP00000422683.1:n.852+26T>C | |
| ENST00000511227.5:c.*1457+26T>C | ENSP00000425226.1:n.*1457+26T>C | |
| ENST00000511325.1:n.570T>C | ||
| ENST00000511526.5:n.1096+26T>C | ||
| NM_014049.4:c.1563+26T>C | NP_054768.2:n.1563+26T>C | |
| NR_033426.1:n.1941+26T>C | ||
| XM_011512742.1:c.1194+26T>C | XP_011511044.1:n.1194+26T>C | |
| XM_024453484.1:c.1194+26T>C | XP_024309252.1:n.1194+26T>C | |
| XM_024453485.1:c.1194+26T>C | XP_024309253.1:n.1194+26T>C | |
| XR_427367.3:n.1639+26T>C | ||
| NM_014049.5:c.1563+26T>C MANE Select | NP_054768.2:n.1563+26T>C | |
| NR_033426.2:n.1811+26T>C |