Linked Data
dbSNP Id:
rs746081219
ExAC:
1:67852252 A / C
gnomAD v2:
1-67852252-A-C
gnomAD v4:
1-67386569-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67386569A>C , CM000663.2:g.67386569A>C | GRCh38 |
| NC_000001.10:g.67852252A>C , CM000663.1:g.67852252A>C | GRCh37 |
| NC_000001.9:g.67624840A>C | NCBI36 |
| NG_032977.1:g.84206A>C | |
| NG_032977.2:g.84219A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696754.1:c.1855+6446A>C | ENSP00000512852.1:n.1855+6446A>C | |
| ENST00000696755.1:c.1855+6446A>C | ENSP00000512853.1:n.1855+6446A>C | |
| ENST00000696757.1:c.1856-10A>C | ENSP00000512854.1:n.1856-10A>C | |
| ENST00000696758.1:c.*1044-3460A>C | ENSP00000512855.1:n.*1044-3460A>C | |
| ENST00000696759.1:c.1856-3460A>C | ENSP00000512856.1:n.1856-3460A>C | |
| ENST00000696763.1:n.948-10A>C | ||
| ENST00000541374.6:c.1597+6446A>C | ENSP00000445276.3:n.1597+6446A>C | |
| ENST00000648487.1:c.1856-10A>C | ENSP00000497959.1:n.1856-10A>C | |
| ENST00000674203.2:c.1856-10A>C MANE Select | ENSP00000501329.1:n.1856-10A>C | |
| ENST00000262345.5:c.1856-10A>C | ENSP00000262345.1:n.1856-10A>C | |
| ENST00000371000.5:c.1856-10A>C | ENSP00000360039.1:n.1856-10A>C | |
| ENST00000465396.1:n.197-10A>C | ||
| ENST00000541374.5:c.1855+6446A>C | ENSP00000445276.2:n.1855+6446A>C | |
| ENST00000544434.5:c.1598-10A>C | ENSP00000442443.1:n.1598-10A>C | |
| NM_001258214.1:c.1856-10A>C | NP_001245143.1:n.1856-10A>C | |
| NM_001258215.1:c.1598-10A>C | NP_001245144.1:n.1598-10A>C | |
| NM_001258216.1:c.1855+6446A>C | NP_001245145.1:n.1855+6446A>C | |
| NM_001559.2:c.1856-10A>C | NP_001550.1:n.1856-10A>C | |
| NR_047583.1:n.2337-3460A>C | ||
| NR_047584.1:n.2496-10A>C | ||
| XM_005270825.1:c.1856-10A>C | XP_005270882.1:n.1856-10A>C | |
| XM_005270827.1:c.1856-10A>C | XP_005270884.1:n.1856-10A>C | |
| XM_005270828.2:c.1856-10A>C | XP_005270885.1:n.1856-10A>C | |
| XM_006710617.1:c.1598-10A>C | XP_006710680.1:n.1598-10A>C | |
| XM_011541383.1:c.1856-10A>C | XP_011539685.1:n.1856-10A>C | |
| XM_011541384.1:c.1697-10A>C | XP_011539686.1:n.1697-10A>C | |
| XM_011541385.1:c.1856-10A>C | XP_011539687.1:n.1856-10A>C | |
| NM_001319233.1:c.1856-10A>C | NP_001306162.1:n.1856-10A>C | |
| XM_005270825.2:c.1856-10A>C | XP_005270882.1:n.1856-10A>C | |
| XM_005270827.2:c.1856-10A>C | XP_005270884.1:n.1856-10A>C | |
| XM_005270828.3:c.1856-10A>C | XP_005270885.1:n.1856-10A>C | |
| XM_006710617.2:c.1598-10A>C | XP_006710680.1:n.1598-10A>C | |
| XM_011541383.2:c.1856-10A>C | XP_011539685.1:n.1856-10A>C | |
| XM_011541384.2:c.1697-10A>C | XP_011539686.1:n.1697-10A>C | |
| XM_017001203.1:c.1856-10A>C | XP_016856692.1:n.1856-10A>C | |
| NM_001374259.2:c.1856-10A>C MANE Select | NP_001361188.1:n.1856-10A>C | |
| NM_001559.3:c.1856-10A>C | NP_001550.1:n.1856-10A>C |