Canonical Allele Identifier: CA468627816
Gene: CACNB2 HGNC NCBI
NSUN6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.18828290C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.18539361C>T , CM000672.2:g.18539361C>T GRCh38
NC_000010.10:g.18828290C>T , CM000672.1:g.18828290C>T GRCh37
NC_000010.9:g.18868296C>T NCBI36
NG_016195.1:g.403685C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377315.6:c.1476C>T (CACNB2) ENSP00000366532.4:p.Asn492=
ENST00000377319.9:c.1341C>T (CACNB2) ENSP00000366536.3:p.Asn447=
ENST00000645287.2:c.1464C>T (CACNB2) ENSP00000496203.1:p.Asn488=
ENST00000282343.13:c.1536C>T (CACNB2) ENSP00000282343.8:p.Asn512=
ENST00000324631.13:c.1620C>T (CACNB2) MANE Select ENSP00000320025.8:p.Asn540=
ENST00000377315.5:c.1476C>T (CACNB2) ENSP00000366532.4:p.Asn492=
ENST00000377319.8:c.1341C>T (CACNB2) ENSP00000366536.3:p.Asn447=
ENST00000377329.10:c.1458C>T (CACNB2) MANE Plus Clinical ENSP00000366546.4:p.Asn486=
ENST00000377331.8:c.1245C>T (CACNB2) ENSP00000366548.4:p.Asn415=
ENST00000643096.2:c.1422C>T (CACNB2) ENSP00000494209.2:p.Asn474=
ENST00000645287.1:c.1464C>T (CACNB2) ENSP00000496203.1:p.Asn488=
ENST00000647168.2:c.*761C>T (CACNB2) ENSP00000495854.2:n.*761C>T
ENST00000650685.1:c.1362C>T (CACNB2) ENSP00000498460.1:p.Asn454=
ENST00000651330.1:c.*894C>T (CACNB2) ENSP00000498457.1:n.*894C>T
ENST00000651468.1:c.1177C>T (CACNB2) ENSP00000498352.1:n.1177C>T
ENST00000651928.1:c.*859C>T (CACNB2) ENSP00000499177.1:n.*859C>T
ENST00000652391.1:c.1440C>T (CACNB2) ENSP00000498938.1:p.Asn480=
ENST00000652478.1:c.*720C>T (CACNB2) ENSP00000498812.1:n.*720C>T
ENST00000282343.12:c.1536C>T (CACNB2) ENSP00000282343.8:p.Asn512=
ENST00000324631.11:c.1620C>T (CACNB2) ENSP00000320025.7:p.Asn540=
ENST00000352115.10:c.1548C>T (CACNB2) ENSP00000344474.6:p.Asn516=
ENST00000377315.4:c.1476C>T (CACNB2) ENSP00000366532.4:p.Asn492=
ENST00000377319.7:c.1341C>T (CACNB2) ENSP00000366536.3:p.Asn447=
ENST00000377328.5:c.870C>T (CACNB2) ENSP00000366545.1:p.Asn290=
ENST00000377329.8:c.1458C>T (CACNB2) ENSP00000366546.4:p.Asn486=
ENST00000377331.6:c.1464C>T (CACNB2) ENSP00000366548.2:p.Asn488=
ENST00000396576.6:c.1455C>T (CACNB2) ENSP00000379821.2:p.Asn485=
ENST00000612134.4:c.1324C>T (CACNB2) ENSP00000480563.1:n.1324C>T
ENST00000612743.1:c.132C>T (CACNB2) ENSP00000478676.1:p.Asn44=
ENST00000615785.4:c.705C>T (CACNB2) ENSP00000480260.1:p.Asn235=
ENST00000617363.4:c.1383C>T (CACNB2) ENSP00000479756.1:p.Asn461=
NM_000724.3:c.1455C>T (CACNB2) NP_000715.2:p.Asn485=
NM_001167945.1:c.1422C>T (CACNB2) NP_001161417.1:p.Asn474=
NM_201570.2:c.1476C>T (CACNB2) NP_963864.1:p.Asn492=
NM_201571.3:c.1536C>T (CACNB2) NP_963865.2:p.Asn512=
NM_201572.3:c.1464C>T (CACNB2) NP_963866.2:p.Asn488=
NM_201590.2:c.1458C>T (CACNB2) NP_963884.2:p.Asn486=
NM_201593.2:c.1506C>T (CACNB2) NP_963887.2:p.Asn502=
NM_201596.2:c.1620C>T (CACNB2) NP_963890.2:p.Asn540=
NM_201597.2:c.1548C>T (CACNB2) NP_963891.1:p.Asn516=
XM_005252588.2:c.1362C>T (CACNB2) XP_005252645.1:p.Asn454=
XM_005252591.2:c.780C>T (CACNB2) XP_005252648.1:p.Asn260=
XM_006717502.2:c.1440C>T (CACNB2) XP_006717565.1:p.Asn480=
XM_011519659.1:c.1386C>T (CACNB2) XP_011517961.1:p.Asn462=
XM_011519660.1:c.1341C>T (CACNB2) XP_011517962.1:p.Asn447=
NM_001330060.1:c.1341C>T (CACNB2) NP_001316989.1:p.Asn447=
XM_005252588.4:c.1362C>T (CACNB2) XP_005252645.1:p.Asn454=
XM_005252591.3:c.780C>T (CACNB2) XP_005252648.1:p.Asn260=
XM_006717502.3:c.1440C>T (CACNB2) XP_006717565.1:p.Asn480=
XM_011519659.2:c.1386C>T (CACNB2) XP_011517961.1:p.Asn462=
XM_017016625.1:c.780C>T (CACNB2) XP_016872114.1:p.Asn260=
XR_001747060.1:n.2423+2708G>A (NSUN6)
XR_001747198.1:n.1745C>T (CACNB2)
NM_000724.4:c.1455C>T (CACNB2) NP_000715.2:p.Asn485=
NM_001167945.2:c.1422C>T (CACNB2) NP_001161417.1:p.Asn474=
NM_001330060.2:c.1341C>T (CACNB2) NP_001316989.1:p.Asn447=
NM_201570.3:c.1476C>T (CACNB2) NP_963864.1:p.Asn492=
NM_201571.4:c.1536C>T (CACNB2) NP_963865.2:p.Asn512=
NM_201572.4:c.1464C>T (CACNB2) NP_963866.2:p.Asn488=
NM_201590.3:c.1458C>T (CACNB2) MANE Plus Clinical NP_963884.2:p.Asn486=
NM_201593.3:c.1506C>T (CACNB2) NP_963887.2:p.Asn502=
NM_201596.3:c.1620C>T (CACNB2) MANE Select NP_963890.2:p.Asn540=
NM_201597.3:c.1548C>T (CACNB2) NP_963891.1:p.Asn516=