Linked Data
ClinVar Variation Id:
1941981
ClinVar RCV Id:
RCV002653696
dbSNP Id:
rs762804748
ExAC:
10:18828452 C / T
gnomAD v2:
10-18828452-C-T
gnomAD v3:
10-18539523-C-T
gnomAD v4:
10-18539523-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.18539523C>T , CM000672.2:g.18539523C>T | GRCh38 |
| NC_000010.10:g.18828452C>T , CM000672.1:g.18828452C>T | GRCh37 |
| NC_000010.9:g.18868458C>T | NCBI36 |
| NG_016195.1:g.403847C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377315.6:c.1638C>T (CACNB2) | ENSP00000366532.4:p.Thr546= | |
| ENST00000377319.9:c.1503C>T (CACNB2) | ENSP00000366536.3:p.Thr501= | |
| ENST00000645287.2:c.1626C>T (CACNB2) | ENSP00000496203.1:p.Thr542= | |
| ENST00000282343.13:c.1698C>T (CACNB2) | ENSP00000282343.8:p.Thr566= | |
| ENST00000324631.13:c.1782C>T (CACNB2) MANE Select | ENSP00000320025.8:p.Thr594= | |
| ENST00000377315.5:c.1638C>T (CACNB2) | ENSP00000366532.4:p.Thr546= | |
| ENST00000377319.8:c.1503C>T (CACNB2) | ENSP00000366536.3:p.Thr501= | |
| ENST00000377329.10:c.1620C>T (CACNB2) MANE Plus Clinical | ENSP00000366546.4:p.Thr540= | |
| ENST00000377331.8:c.1407C>T (CACNB2) | ENSP00000366548.4:p.Thr469= | |
| ENST00000643096.2:c.1584C>T (CACNB2) | ENSP00000494209.2:p.Thr528= | |
| ENST00000645287.1:c.1626C>T (CACNB2) | ENSP00000496203.1:p.Thr542= | |
| ENST00000647168.2:c.*923C>T (CACNB2) | ENSP00000495854.2:n.*923C>T | |
| ENST00000650685.1:c.1524C>T (CACNB2) | ENSP00000498460.1:p.Thr508= | |
| ENST00000651330.1:c.*1056C>T (CACNB2) | ENSP00000498457.1:n.*1056C>T | |
| ENST00000651468.1:c.1339C>T (CACNB2) | ENSP00000498352.1:n.1339C>T | |
| ENST00000651928.1:c.*1021C>T (CACNB2) | ENSP00000499177.1:n.*1021C>T | |
| ENST00000652391.1:c.1602C>T (CACNB2) | ENSP00000498938.1:p.Thr534= | |
| ENST00000652478.1:c.*882C>T (CACNB2) | ENSP00000498812.1:n.*882C>T | |
| ENST00000282343.12:c.1698C>T (CACNB2) | ENSP00000282343.8:p.Thr566= | |
| ENST00000324631.11:c.1782C>T (CACNB2) | ENSP00000320025.7:p.Thr594= | |
| ENST00000352115.10:c.1710C>T (CACNB2) | ENSP00000344474.6:p.Thr570= | |
| ENST00000377315.4:c.1638C>T (CACNB2) | ENSP00000366532.4:p.Thr546= | |
| ENST00000377319.7:c.1503C>T (CACNB2) | ENSP00000366536.3:p.Thr501= | |
| ENST00000377328.5:c.1032C>T (CACNB2) | ENSP00000366545.1:p.Thr344= | |
| ENST00000377329.8:c.1620C>T (CACNB2) | ENSP00000366546.4:p.Thr540= | |
| ENST00000377331.6:c.1626C>T (CACNB2) | ENSP00000366548.2:p.Thr542= | |
| ENST00000396576.6:c.1617C>T (CACNB2) | ENSP00000379821.2:p.Thr539= | |
| ENST00000612134.4:c.1486C>T (CACNB2) | ENSP00000480563.1:n.1486C>T | |
| ENST00000612743.1:c.294C>T (CACNB2) | ENSP00000478676.1:p.Thr98= | |
| ENST00000615785.4:c.867C>T (CACNB2) | ENSP00000480260.1:p.Thr289= | |
| ENST00000617363.4:c.1545C>T (CACNB2) | ENSP00000479756.1:p.Thr515= | |
| NM_000724.3:c.1617C>T (CACNB2) | NP_000715.2:p.Thr539= | |
| NM_001167945.1:c.1584C>T (CACNB2) | NP_001161417.1:p.Thr528= | |
| NM_201570.2:c.1638C>T (CACNB2) | NP_963864.1:p.Thr546= | |
| NM_201571.3:c.1698C>T (CACNB2) | NP_963865.2:p.Thr566= | |
| NM_201572.3:c.1626C>T (CACNB2) | NP_963866.2:p.Thr542= | |
| NM_201590.2:c.1620C>T (CACNB2) | NP_963884.2:p.Thr540= | |
| NM_201593.2:c.1668C>T (CACNB2) | NP_963887.2:p.Thr556= | |
| NM_201596.2:c.1782C>T (CACNB2) | NP_963890.2:p.Thr594= | |
| NM_201597.2:c.1710C>T (CACNB2) | NP_963891.1:p.Thr570= | |
| XM_005252588.2:c.1524C>T (CACNB2) | XP_005252645.1:p.Thr508= | |
| XM_005252591.2:c.942C>T (CACNB2) | XP_005252648.1:p.Thr314= | |
| XM_006717502.2:c.1602C>T (CACNB2) | XP_006717565.1:p.Thr534= | |
| XM_011519659.1:c.1548C>T (CACNB2) | XP_011517961.1:p.Thr516= | |
| XM_011519660.1:c.1503C>T (CACNB2) | XP_011517962.1:p.Thr501= | |
| NM_001330060.1:c.1503C>T (CACNB2) | NP_001316989.1:p.Thr501= | |
| XM_005252588.4:c.1524C>T (CACNB2) | XP_005252645.1:p.Thr508= | |
| XM_005252591.3:c.942C>T (CACNB2) | XP_005252648.1:p.Thr314= | |
| XM_006717502.3:c.1602C>T (CACNB2) | XP_006717565.1:p.Thr534= | |
| XM_011519659.2:c.1548C>T (CACNB2) | XP_011517961.1:p.Thr516= | |
| XM_017016625.1:c.942C>T (CACNB2) | XP_016872114.1:p.Thr314= | |
| XR_001747060.1:n.2423+2546G>A (NSUN6) | ||
| XR_001747198.1:n.1907C>T (CACNB2) | ||
| NM_000724.4:c.1617C>T (CACNB2) | NP_000715.2:p.Thr539= | |
| NM_001167945.2:c.1584C>T (CACNB2) | NP_001161417.1:p.Thr528= | |
| NM_001330060.2:c.1503C>T (CACNB2) | NP_001316989.1:p.Thr501= | |
| NM_201570.3:c.1638C>T (CACNB2) | NP_963864.1:p.Thr546= | |
| NM_201571.4:c.1698C>T (CACNB2) | NP_963865.2:p.Thr566= | |
| NM_201572.4:c.1626C>T (CACNB2) | NP_963866.2:p.Thr542= | |
| NM_201590.3:c.1620C>T (CACNB2) MANE Plus Clinical | NP_963884.2:p.Thr540= | |
| NM_201593.3:c.1668C>T (CACNB2) | NP_963887.2:p.Thr556= | |
| NM_201596.3:c.1782C>T (CACNB2) MANE Select | NP_963890.2:p.Thr594= | |
| NM_201597.3:c.1710C>T (CACNB2) | NP_963891.1:p.Thr570= |