Linked Data
ClinVar Variation Id:
2917081
ClinVar RCV Id:
RCV003622344
dbSNP Id:
rs772557073
ExAC:
10:18828423 C / G
gnomAD v2:
10-18828423-C-G
gnomAD v3:
10-18539494-C-G
gnomAD v4:
10-18539494-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.18539494C>G , CM000672.2:g.18539494C>G | GRCh38 |
| NC_000010.10:g.18828423C>G , CM000672.1:g.18828423C>G | GRCh37 |
| NC_000010.9:g.18868429C>G | NCBI36 |
| NG_016195.1:g.403818C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377315.6:c.1609C>G (CACNB2) | ENSP00000366532.4:p.His537Asp | |
| ENST00000377319.9:c.1474C>G (CACNB2) | ENSP00000366536.3:p.His492Asp | |
| ENST00000645287.2:c.1597C>G (CACNB2) | ENSP00000496203.1:p.His533Asp | |
| ENST00000282343.13:c.1669C>G (CACNB2) | ENSP00000282343.8:p.His557Asp | |
| ENST00000324631.13:c.1753C>G (CACNB2) MANE Select | ENSP00000320025.8:p.His585Asp | |
| ENST00000377315.5:c.1609C>G (CACNB2) | ENSP00000366532.4:p.His537Asp | |
| ENST00000377319.8:c.1474C>G (CACNB2) | ENSP00000366536.3:p.His492Asp | |
| ENST00000377329.10:c.1591C>G (CACNB2) MANE Plus Clinical | ENSP00000366546.4:p.His531Asp | |
| ENST00000377331.8:c.1378C>G (CACNB2) | ENSP00000366548.4:p.His460Asp | |
| ENST00000643096.2:c.1555C>G (CACNB2) | ENSP00000494209.2:p.His519Asp | |
| ENST00000645287.1:c.1597C>G (CACNB2) | ENSP00000496203.1:p.His533Asp | |
| ENST00000647168.2:c.*894C>G (CACNB2) | ENSP00000495854.2:n.*894C>G | |
| ENST00000650685.1:c.1495C>G (CACNB2) | ENSP00000498460.1:p.His499Asp | |
| ENST00000651330.1:c.*1027C>G (CACNB2) | ENSP00000498457.1:n.*1027C>G | |
| ENST00000651468.1:c.1310C>G (CACNB2) | ENSP00000498352.1:n.1310C>G | |
| ENST00000651928.1:c.*992C>G (CACNB2) | ENSP00000499177.1:n.*992C>G | |
| ENST00000652391.1:c.1573C>G (CACNB2) | ENSP00000498938.1:p.His525Asp | |
| ENST00000652478.1:c.*853C>G (CACNB2) | ENSP00000498812.1:n.*853C>G | |
| ENST00000282343.12:c.1669C>G (CACNB2) | ENSP00000282343.8:p.His557Asp | |
| ENST00000324631.11:c.1753C>G (CACNB2) | ENSP00000320025.7:p.His585Asp | |
| ENST00000352115.10:c.1681C>G (CACNB2) | ENSP00000344474.6:p.His561Asp | |
| ENST00000377315.4:c.1609C>G (CACNB2) | ENSP00000366532.4:p.His537Asp | |
| ENST00000377319.7:c.1474C>G (CACNB2) | ENSP00000366536.3:p.His492Asp | |
| ENST00000377328.5:c.1003C>G (CACNB2) | ENSP00000366545.1:p.His335Asp | |
| ENST00000377329.8:c.1591C>G (CACNB2) | ENSP00000366546.4:p.His531Asp | |
| ENST00000377331.6:c.1597C>G (CACNB2) | ENSP00000366548.2:p.His533Asp | |
| ENST00000396576.6:c.1588C>G (CACNB2) | ENSP00000379821.2:p.His530Asp | |
| ENST00000612134.4:c.1457C>G (CACNB2) | ENSP00000480563.1:n.1457C>G | |
| ENST00000612743.1:c.265C>G (CACNB2) | ENSP00000478676.1:p.His89Asp | |
| ENST00000615785.4:c.838C>G (CACNB2) | ENSP00000480260.1:p.His280Asp | |
| ENST00000617363.4:c.1516C>G (CACNB2) | ENSP00000479756.1:p.His506Asp | |
| NM_000724.3:c.1588C>G (CACNB2) | NP_000715.2:p.His530Asp | |
| NM_001167945.1:c.1555C>G (CACNB2) | NP_001161417.1:p.His519Asp | |
| NM_201570.2:c.1609C>G (CACNB2) | NP_963864.1:p.His537Asp | |
| NM_201571.3:c.1669C>G (CACNB2) | NP_963865.2:p.His557Asp | |
| NM_201572.3:c.1597C>G (CACNB2) | NP_963866.2:p.His533Asp | |
| NM_201590.2:c.1591C>G (CACNB2) | NP_963884.2:p.His531Asp | |
| NM_201593.2:c.1639C>G (CACNB2) | NP_963887.2:p.His547Asp | |
| NM_201596.2:c.1753C>G (CACNB2) | NP_963890.2:p.His585Asp | |
| NM_201597.2:c.1681C>G (CACNB2) | NP_963891.1:p.His561Asp | |
| XM_005252588.2:c.1495C>G (CACNB2) | XP_005252645.1:p.His499Asp | |
| XM_005252591.2:c.913C>G (CACNB2) | XP_005252648.1:p.His305Asp | |
| XM_006717502.2:c.1573C>G (CACNB2) | XP_006717565.1:p.His525Asp | |
| XM_011519659.1:c.1519C>G (CACNB2) | XP_011517961.1:p.His507Asp | |
| XM_011519660.1:c.1474C>G (CACNB2) | XP_011517962.1:p.His492Asp | |
| NM_001330060.1:c.1474C>G (CACNB2) | NP_001316989.1:p.His492Asp | |
| XM_005252588.4:c.1495C>G (CACNB2) | XP_005252645.1:p.His499Asp | |
| XM_005252591.3:c.913C>G (CACNB2) | XP_005252648.1:p.His305Asp | |
| XM_006717502.3:c.1573C>G (CACNB2) | XP_006717565.1:p.His525Asp | |
| XM_011519659.2:c.1519C>G (CACNB2) | XP_011517961.1:p.His507Asp | |
| XM_017016625.1:c.913C>G (CACNB2) | XP_016872114.1:p.His305Asp | |
| XR_001747060.1:n.2423+2575G>C (NSUN6) | ||
| XR_001747198.1:n.1878C>G (CACNB2) | ||
| NM_000724.4:c.1588C>G (CACNB2) | NP_000715.2:p.His530Asp | |
| NM_001167945.2:c.1555C>G (CACNB2) | NP_001161417.1:p.His519Asp | |
| NM_001330060.2:c.1474C>G (CACNB2) | NP_001316989.1:p.His492Asp | |
| NM_201570.3:c.1609C>G (CACNB2) | NP_963864.1:p.His537Asp | |
| NM_201571.4:c.1669C>G (CACNB2) | NP_963865.2:p.His557Asp | |
| NM_201572.4:c.1597C>G (CACNB2) | NP_963866.2:p.His533Asp | |
| NM_201590.3:c.1591C>G (CACNB2) MANE Plus Clinical | NP_963884.2:p.His531Asp | |
| NM_201593.3:c.1639C>G (CACNB2) | NP_963887.2:p.His547Asp | |
| NM_201596.3:c.1753C>G (CACNB2) MANE Select | NP_963890.2:p.His585Asp | |
| NM_201597.3:c.1681C>G (CACNB2) | NP_963891.1:p.His561Asp |