Linked Data
ClinVar Variation Id:
194121
dbSNP Id:
rs557754125
ExAC:
8:38274815 G / A
gnomAD v2:
8-38274815-G-A
gnomAD v3:
8-38417297-G-A
gnomAD v4:
8-38417297-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38417297G>A , CM000670.2:g.38417297G>A | GRCh38 |
| NC_000008.10:g.38274815G>A , CM000670.1:g.38274815G>A | GRCh37 |
| NC_000008.9:g.38393972G>A | NCBI36 |
| NG_007729.1:g.56538C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703405.1:c.1663+9C>T | ENSP00000515291.1:n.1663+9C>T | |
| ENST00000341462.9:c.1651+9C>T | ENSP00000340636.7:n.1651+9C>T | |
| ENST00000425967.8:c.1651+9C>T | ENSP00000393312.4:n.1651+9C>T | |
| ENST00000524528.2:n.2556+9C>T | ||
| ENST00000682398.1:n.438C>T | ||
| ENST00000683765.1:c.1843+9C>T | ENSP00000507039.1:n.1843+9C>T | |
| ENST00000683815.1:c.1651+9C>T | ENSP00000507997.1:n.1651+9C>T | |
| ENST00000683948.1:n.2351+9C>T | ||
| ENST00000684654.1:c.1384+9C>T | ENSP00000507205.1:n.1384+9C>T | |
| ENST00000447712.7:c.1663+9C>T MANE Select | ENSP00000400162.2:n.1663+9C>T | |
| ENST00000649678.1:c.1651+9C>T | ENSP00000497266.1:n.1651+9C>T | |
| ENST00000674189.1:c.*1309+9C>T | ENSP00000501345.1:n.*1309+9C>T | |
| ENST00000674380.1:c.*1630+9C>T | ENSP00000501514.1:n.*1630+9C>T | |
| ENST00000674474.1:n.3157+9C>T | ||
| ENST00000326324.10:c.1390+9C>T | ENSP00000327229.6:n.1390+9C>T | |
| ENST00000335922.9:c.1633+9C>T | ENSP00000337247.5:n.1633+9C>T | |
| ENST00000341462.8:c.*713+9C>T | ENSP00000340636.6:n.*713+9C>T | |
| ENST00000356207.9:c.1396+9C>T | ENSP00000348537.5:n.1396+9C>T | |
| ENST00000397091.9:c.1657+9C>T | ENSP00000380280.5:n.1657+9C>T | |
| ENST00000397103.5:c.1396+9C>T | ENSP00000380292.1:n.1396+9C>T | |
| ENST00000397108.8:c.1657+9C>T | ENSP00000380297.4:n.1657+9C>T | |
| ENST00000397113.6:c.1657+9C>T | ENSP00000380302.2:n.1657+9C>T | |
| ENST00000425967.7:c.1756+9C>T | ENSP00000393312.3:n.1756+9C>T | |
| ENST00000447712.6:c.1663+9C>T | ENSP00000400162.2:n.1663+9C>T | |
| ENST00000487647.5:c.1540+9C>T | ENSP00000435254.1:n.1540+9C>T | |
| ENST00000526570.5:n.3942+9C>T | ||
| ENST00000527114.5:n.1185+9C>T | ||
| ENST00000532791.5:c.1657+9C>T | ENSP00000432972.1:n.1657+9C>T | |
| ENST00000533619.5:n.209+9C>T | ||
| ENST00000619564.3:c.*558+9C>T | ENSP00000484553.1:n.*558+9C>T | |
| NM_001174063.1:c.1657+9C>T | NP_001167534.1:n.1657+9C>T | |
| NM_001174064.1:c.1633+9C>T | NP_001167535.1:n.1633+9C>T | |
| NM_001174065.1:c.1657+9C>T | NP_001167536.1:n.1657+9C>T | |
| NM_001174066.1:c.1396+9C>T | NP_001167537.1:n.1396+9C>T | |
| NM_001174067.1:c.1756+9C>T | NP_001167538.1:n.1756+9C>T | |
| NM_015850.3:c.1657+9C>T | NP_056934.2:n.1657+9C>T | |
| NM_023105.2:c.1396+9C>T | NP_075593.1:n.1396+9C>T | |
| NM_023106.2:c.1390+9C>T | NP_075594.1:n.1390+9C>T | |
| NM_023110.2:c.1663+9C>T | NP_075598.2:n.1663+9C>T | |
| XM_006716303.2:c.1663+9C>T | XP_006716366.1:n.1663+9C>T | |
| XM_006716304.1:c.1663+9C>T | XP_006716367.1:n.1663+9C>T | |
| XM_006716305.2:c.1663+9C>T | XP_006716368.1:n.1663+9C>T | |
| XM_006716306.2:c.1657+9C>T | XP_006716369.1:n.1657+9C>T | |
| XM_006716307.1:c.1657+9C>T | XP_006716370.1:n.1657+9C>T | |
| XM_006716309.2:c.1639+9C>T | XP_006716372.1:n.1639+9C>T | |
| XM_006716310.2:c.1396+9C>T | XP_006716373.1:n.1396+9C>T | |
| XM_006716311.1:c.1396+9C>T | XP_006716374.1:n.1396+9C>T | |
| XM_006716312.1:c.1396+9C>T | XP_006716375.1:n.1396+9C>T | |
| XM_006716313.2:c.1390+9C>T | XP_006716376.1:n.1390+9C>T | |
| XM_006716314.1:c.1390+9C>T | XP_006716377.1:n.1390+9C>T | |
| XM_011544443.1:c.1762+9C>T | XP_011542745.1:n.1762+9C>T | |
| XM_011544444.1:c.1756+9C>T | XP_011542746.1:n.1756+9C>T | |
| XM_011544445.1:c.1756+9C>T | XP_011542747.1:n.1756+9C>T | |
| XM_011544446.1:c.1762+9C>T | XP_011542748.1:n.1762+9C>T | |
| XM_011544447.1:c.1756+9C>T | XP_011542749.1:n.1756+9C>T | |
| XM_011544448.1:c.1495+9C>T | XP_011542750.1:n.1495+9C>T | |
| XM_011544449.1:c.1489+9C>T | XP_011542751.1:n.1489+9C>T | |
| XM_011544450.1:c.1489+9C>T | XP_011542752.1:n.1489+9C>T | |
| XM_011544451.1:c.1372+9C>T | XP_011542753.1:n.1372+9C>T | |
| NM_001354367.1:c.1657+9C>T | NP_001341296.1:n.1657+9C>T | |
| NM_001354368.1:c.1384+9C>T | NP_001341297.1:n.1384+9C>T | |
| NM_001354369.1:c.1651+9C>T | NP_001341298.1:n.1651+9C>T | |
| NM_001354370.1:c.1390+9C>T | NP_001341299.1:n.1390+9C>T | |
| XM_006716303.3:c.1663+9C>T | XP_006716366.1:n.1663+9C>T | |
| XM_006716310.3:c.1396+9C>T | XP_006716373.1:n.1396+9C>T | |
| XM_006716312.2:c.1396+9C>T | XP_006716375.1:n.1396+9C>T | |
| XM_006716314.2:c.1390+9C>T | XP_006716377.1:n.1390+9C>T | |
| XM_011544443.2:c.1762+9C>T | XP_011542745.1:n.1762+9C>T | |
| XM_011544445.2:c.1756+9C>T | XP_011542747.1:n.1756+9C>T | |
| XM_011544446.2:c.1762+9C>T | XP_011542748.1:n.1762+9C>T | |
| XM_011544447.2:c.1756+9C>T | XP_011542749.1:n.1756+9C>T | |
| XM_011544450.2:c.1489+9C>T | XP_011542752.1:n.1489+9C>T | |
| XM_017013219.1:c.1750+9C>T | XP_016868708.1:n.1750+9C>T | |
| XM_017013220.1:c.1750+9C>T | XP_016868709.1:n.1750+9C>T | |
| XM_017013221.1:c.1663+9C>T | XP_016868710.1:n.1663+9C>T | |
| XM_017013222.2:c.1657+9C>T | XP_016868711.1:n.1657+9C>T | |
| XM_017013224.2:c.1651+9C>T | XP_016868713.1:n.1651+9C>T | |
| XM_017013225.2:c.1651+9C>T | XP_016868714.1:n.1651+9C>T | |
| XM_017013226.1:c.1489+9C>T | XP_016868715.1:n.1489+9C>T | |
| XM_017013227.1:c.1483+9C>T | XP_016868716.1:n.1483+9C>T | |
| XM_017013229.2:c.691+9C>T | XP_016868718.1:n.691+9C>T | |
| XM_017013230.1:c.691+9C>T | XP_016868719.1:n.691+9C>T | |
| XM_024447097.1:c.1639+9C>T | XP_024302865.1:n.1639+9C>T | |
| XR_001745495.1:n.1911+9C>T | ||
| XR_001745496.1:n.1911+9C>T | ||
| NM_001174063.2:c.1657+9C>T | NP_001167534.1:n.1657+9C>T | |
| NM_001174064.2:c.1633+9C>T | NP_001167535.1:n.1633+9C>T | |
| NM_001174065.2:c.1657+9C>T | NP_001167536.1:n.1657+9C>T | |
| NM_001174066.2:c.1396+9C>T | NP_001167537.1:n.1396+9C>T | |
| NM_001354368.2:c.1384+9C>T | NP_001341297.1:n.1384+9C>T | |
| NM_015850.4:c.1657+9C>T | NP_056934.2:n.1657+9C>T | |
| NM_023105.3:c.1396+9C>T | NP_075593.1:n.1396+9C>T | |
| NM_023106.3:c.1390+9C>T | NP_075594.1:n.1390+9C>T | |
| NM_023110.3:c.1663+9C>T MANE Select | NP_075598.2:n.1663+9C>T | |
| NM_001174067.2:c.1756+9C>T | NP_001167538.1:n.1756+9C>T | |
| NM_001354367.2:c.1657+9C>T | NP_001341296.1:n.1657+9C>T | |
| NM_001354369.2:c.1651+9C>T | NP_001341298.1:n.1651+9C>T | |
| NM_001354370.2:c.1390+9C>T | NP_001341299.1:n.1390+9C>T |