Linked Data
ClinVar Variation Id:
416838
dbSNP Id:
rs144182966
ExAC:
10:18828446 C / T
gnomAD v2:
10-18828446-C-T
gnomAD v3:
10-18539517-C-T
gnomAD v4:
10-18539517-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.18539517C>T , CM000672.2:g.18539517C>T | GRCh38 |
| NC_000010.10:g.18828446C>T , CM000672.1:g.18828446C>T | GRCh37 |
| NC_000010.9:g.18868452C>T | NCBI36 |
| NG_016195.1:g.403841C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377315.6:c.1632C>T (CACNB2) | ENSP00000366532.4:p.Asp544= | |
| ENST00000377319.9:c.1497C>T (CACNB2) | ENSP00000366536.3:p.Asp499= | |
| ENST00000645287.2:c.1620C>T (CACNB2) | ENSP00000496203.1:p.Asp540= | |
| ENST00000282343.13:c.1692C>T (CACNB2) | ENSP00000282343.8:p.Asp564= | |
| ENST00000324631.13:c.1776C>T (CACNB2) MANE Select | ENSP00000320025.8:p.Asp592= | |
| ENST00000377315.5:c.1632C>T (CACNB2) | ENSP00000366532.4:p.Asp544= | |
| ENST00000377319.8:c.1497C>T (CACNB2) | ENSP00000366536.3:p.Asp499= | |
| ENST00000377329.10:c.1614C>T (CACNB2) MANE Plus Clinical | ENSP00000366546.4:p.Asp538= | |
| ENST00000377331.8:c.1401C>T (CACNB2) | ENSP00000366548.4:p.Asp467= | |
| ENST00000643096.2:c.1578C>T (CACNB2) | ENSP00000494209.2:p.Asp526= | |
| ENST00000645287.1:c.1620C>T (CACNB2) | ENSP00000496203.1:p.Asp540= | |
| ENST00000647168.2:c.*917C>T (CACNB2) | ENSP00000495854.2:n.*917C>T | |
| ENST00000650685.1:c.1518C>T (CACNB2) | ENSP00000498460.1:p.Asp506= | |
| ENST00000651330.1:c.*1050C>T (CACNB2) | ENSP00000498457.1:n.*1050C>T | |
| ENST00000651468.1:c.1333C>T (CACNB2) | ENSP00000498352.1:n.1333C>T | |
| ENST00000651928.1:c.*1015C>T (CACNB2) | ENSP00000499177.1:n.*1015C>T | |
| ENST00000652391.1:c.1596C>T (CACNB2) | ENSP00000498938.1:p.Asp532= | |
| ENST00000652478.1:c.*876C>T (CACNB2) | ENSP00000498812.1:n.*876C>T | |
| ENST00000282343.12:c.1692C>T (CACNB2) | ENSP00000282343.8:p.Asp564= | |
| ENST00000324631.11:c.1776C>T (CACNB2) | ENSP00000320025.7:p.Asp592= | |
| ENST00000352115.10:c.1704C>T (CACNB2) | ENSP00000344474.6:p.Asp568= | |
| ENST00000377315.4:c.1632C>T (CACNB2) | ENSP00000366532.4:p.Asp544= | |
| ENST00000377319.7:c.1497C>T (CACNB2) | ENSP00000366536.3:p.Asp499= | |
| ENST00000377328.5:c.1026C>T (CACNB2) | ENSP00000366545.1:p.Asp342= | |
| ENST00000377329.8:c.1614C>T (CACNB2) | ENSP00000366546.4:p.Asp538= | |
| ENST00000377331.6:c.1620C>T (CACNB2) | ENSP00000366548.2:p.Asp540= | |
| ENST00000396576.6:c.1611C>T (CACNB2) | ENSP00000379821.2:p.Asp537= | |
| ENST00000612134.4:c.1480C>T (CACNB2) | ENSP00000480563.1:n.1480C>T | |
| ENST00000612743.1:c.288C>T (CACNB2) | ENSP00000478676.1:p.Asp96= | |
| ENST00000615785.4:c.861C>T (CACNB2) | ENSP00000480260.1:p.Asp287= | |
| ENST00000617363.4:c.1539C>T (CACNB2) | ENSP00000479756.1:p.Asp513= | |
| NM_000724.3:c.1611C>T (CACNB2) | NP_000715.2:p.Asp537= | |
| NM_001167945.1:c.1578C>T (CACNB2) | NP_001161417.1:p.Asp526= | |
| NM_201570.2:c.1632C>T (CACNB2) | NP_963864.1:p.Asp544= | |
| NM_201571.3:c.1692C>T (CACNB2) | NP_963865.2:p.Asp564= | |
| NM_201572.3:c.1620C>T (CACNB2) | NP_963866.2:p.Asp540= | |
| NM_201590.2:c.1614C>T (CACNB2) | NP_963884.2:p.Asp538= | |
| NM_201593.2:c.1662C>T (CACNB2) | NP_963887.2:p.Asp554= | |
| NM_201596.2:c.1776C>T (CACNB2) | NP_963890.2:p.Asp592= | |
| NM_201597.2:c.1704C>T (CACNB2) | NP_963891.1:p.Asp568= | |
| XM_005252588.2:c.1518C>T (CACNB2) | XP_005252645.1:p.Asp506= | |
| XM_005252591.2:c.936C>T (CACNB2) | XP_005252648.1:p.Asp312= | |
| XM_006717502.2:c.1596C>T (CACNB2) | XP_006717565.1:p.Asp532= | |
| XM_011519659.1:c.1542C>T (CACNB2) | XP_011517961.1:p.Asp514= | |
| XM_011519660.1:c.1497C>T (CACNB2) | XP_011517962.1:p.Asp499= | |
| NM_001330060.1:c.1497C>T (CACNB2) | NP_001316989.1:p.Asp499= | |
| XM_005252588.4:c.1518C>T (CACNB2) | XP_005252645.1:p.Asp506= | |
| XM_005252591.3:c.936C>T (CACNB2) | XP_005252648.1:p.Asp312= | |
| XM_006717502.3:c.1596C>T (CACNB2) | XP_006717565.1:p.Asp532= | |
| XM_011519659.2:c.1542C>T (CACNB2) | XP_011517961.1:p.Asp514= | |
| XM_017016625.1:c.936C>T (CACNB2) | XP_016872114.1:p.Asp312= | |
| XR_001747060.1:n.2423+2552G>A (NSUN6) | ||
| XR_001747198.1:n.1901C>T (CACNB2) | ||
| NM_000724.4:c.1611C>T (CACNB2) | NP_000715.2:p.Asp537= | |
| NM_001167945.2:c.1578C>T (CACNB2) | NP_001161417.1:p.Asp526= | |
| NM_001330060.2:c.1497C>T (CACNB2) | NP_001316989.1:p.Asp499= | |
| NM_201570.3:c.1632C>T (CACNB2) | NP_963864.1:p.Asp544= | |
| NM_201571.4:c.1692C>T (CACNB2) | NP_963865.2:p.Asp564= | |
| NM_201572.4:c.1620C>T (CACNB2) | NP_963866.2:p.Asp540= | |
| NM_201590.3:c.1614C>T (CACNB2) MANE Plus Clinical | NP_963884.2:p.Asp538= | |
| NM_201593.3:c.1662C>T (CACNB2) | NP_963887.2:p.Asp554= | |
| NM_201596.3:c.1776C>T (CACNB2) MANE Select | NP_963890.2:p.Asp592= | |
| NM_201597.3:c.1704C>T (CACNB2) | NP_963891.1:p.Asp568= |