Canonical Allele Identifier: CA376071512

Gene: CACNB2 NSUN6

Linked Data

• MyVariant Identifiers: chr10:g.18828289A>C (hg19) ; chr10:g.18539360A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539360A>C , CM000672.2:g.18539360A>C	GRCh38
NC_000010.10:g.18828289A>C , CM000672.1:g.18828289A>C	GRCh37
NC_000010.9:g.18868295A>C	NCBI36
NG_016195.1:g.403684A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1475A>C (CACNB2)	ENSP00000366532.4:p.Asn492Thr
ENST00000377319.9:c.1340A>C (CACNB2)	ENSP00000366536.3:p.Asn447Thr
ENST00000645287.2:c.1463A>C (CACNB2)	ENSP00000496203.1:p.Asn488Thr
ENST00000282343.13:c.1535A>C (CACNB2)	ENSP00000282343.8:p.Asn512Thr
ENST00000324631.13:c.1619A>C (CACNB2) MANE Select	ENSP00000320025.8:p.Asn540Thr
ENST00000377315.5:c.1475A>C (CACNB2)	ENSP00000366532.4:p.Asn492Thr
ENST00000377319.8:c.1340A>C (CACNB2)	ENSP00000366536.3:p.Asn447Thr
ENST00000377329.10:c.1457A>C (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Asn486Thr
ENST00000377331.8:c.1244A>C (CACNB2)	ENSP00000366548.4:p.Asn415Thr
ENST00000643096.2:c.1421A>C (CACNB2)	ENSP00000494209.2:p.Asn474Thr
ENST00000645287.1:c.1463A>C (CACNB2)	ENSP00000496203.1:p.Asn488Thr
ENST00000647168.2:c.*760A>C (CACNB2)	ENSP00000495854.2:n.*760A>C
ENST00000650685.1:c.1361A>C (CACNB2)	ENSP00000498460.1:p.Asn454Thr
ENST00000651330.1:c.*893A>C (CACNB2)	ENSP00000498457.1:n.*893A>C
ENST00000651468.1:c.1176A>C (CACNB2)	ENSP00000498352.1:n.1176A>C
ENST00000651928.1:c.*858A>C (CACNB2)	ENSP00000499177.1:n.*858A>C
ENST00000652391.1:c.1439A>C (CACNB2)	ENSP00000498938.1:p.Asn480Thr
ENST00000652478.1:c.*719A>C (CACNB2)	ENSP00000498812.1:n.*719A>C
ENST00000282343.12:c.1535A>C (CACNB2)	ENSP00000282343.8:p.Asn512Thr
ENST00000324631.11:c.1619A>C (CACNB2)	ENSP00000320025.7:p.Asn540Thr
ENST00000352115.10:c.1547A>C (CACNB2)	ENSP00000344474.6:p.Asn516Thr
ENST00000377315.4:c.1475A>C (CACNB2)	ENSP00000366532.4:p.Asn492Thr
ENST00000377319.7:c.1340A>C (CACNB2)	ENSP00000366536.3:p.Asn447Thr
ENST00000377328.5:c.869A>C (CACNB2)	ENSP00000366545.1:p.Asn290Thr
ENST00000377329.8:c.1457A>C (CACNB2)	ENSP00000366546.4:p.Asn486Thr
ENST00000377331.6:c.1463A>C (CACNB2)	ENSP00000366548.2:p.Asn488Thr
ENST00000396576.6:c.1454A>C (CACNB2)	ENSP00000379821.2:p.Asn485Thr
ENST00000612134.4:c.1323A>C (CACNB2)	ENSP00000480563.1:n.1323A>C
ENST00000612743.1:c.131A>C (CACNB2)	ENSP00000478676.1:p.Asn44Thr
ENST00000615785.4:c.704A>C (CACNB2)	ENSP00000480260.1:p.Asn235Thr
ENST00000617363.4:c.1382A>C (CACNB2)	ENSP00000479756.1:p.Asn461Thr
NM_000724.3:c.1454A>C (CACNB2)	NP_000715.2:p.Asn485Thr
NM_001167945.1:c.1421A>C (CACNB2)	NP_001161417.1:p.Asn474Thr
NM_201570.2:c.1475A>C (CACNB2)	NP_963864.1:p.Asn492Thr
NM_201571.3:c.1535A>C (CACNB2)	NP_963865.2:p.Asn512Thr
NM_201572.3:c.1463A>C (CACNB2)	NP_963866.2:p.Asn488Thr
NM_201590.2:c.1457A>C (CACNB2)	NP_963884.2:p.Asn486Thr
NM_201593.2:c.1505A>C (CACNB2)	NP_963887.2:p.Asn502Thr
NM_201596.2:c.1619A>C (CACNB2)	NP_963890.2:p.Asn540Thr
NM_201597.2:c.1547A>C (CACNB2)	NP_963891.1:p.Asn516Thr
XM_005252588.2:c.1361A>C (CACNB2)	XP_005252645.1:p.Asn454Thr
XM_005252591.2:c.779A>C (CACNB2)	XP_005252648.1:p.Asn260Thr
XM_006717502.2:c.1439A>C (CACNB2)	XP_006717565.1:p.Asn480Thr
XM_011519659.1:c.1385A>C (CACNB2)	XP_011517961.1:p.Asn462Thr
XM_011519660.1:c.1340A>C (CACNB2)	XP_011517962.1:p.Asn447Thr
NM_001330060.1:c.1340A>C (CACNB2)	NP_001316989.1:p.Asn447Thr
XM_005252588.4:c.1361A>C (CACNB2)	XP_005252645.1:p.Asn454Thr
XM_005252591.3:c.779A>C (CACNB2)	XP_005252648.1:p.Asn260Thr
XM_006717502.3:c.1439A>C (CACNB2)	XP_006717565.1:p.Asn480Thr
XM_011519659.2:c.1385A>C (CACNB2)	XP_011517961.1:p.Asn462Thr
XM_017016625.1:c.779A>C (CACNB2)	XP_016872114.1:p.Asn260Thr
XR_001747060.1:n.2423+2709T>G (NSUN6)
XR_001747198.1:n.1744A>C (CACNB2)
NM_000724.4:c.1454A>C (CACNB2)	NP_000715.2:p.Asn485Thr
NM_001167945.2:c.1421A>C (CACNB2)	NP_001161417.1:p.Asn474Thr
NM_001330060.2:c.1340A>C (CACNB2)	NP_001316989.1:p.Asn447Thr
NM_201570.3:c.1475A>C (CACNB2)	NP_963864.1:p.Asn492Thr
NM_201571.4:c.1535A>C (CACNB2)	NP_963865.2:p.Asn512Thr
NM_201572.4:c.1463A>C (CACNB2)	NP_963866.2:p.Asn488Thr
NM_201590.3:c.1457A>C (CACNB2) MANE Plus Clinical	NP_963884.2:p.Asn486Thr
NM_201593.3:c.1505A>C (CACNB2)	NP_963887.2:p.Asn502Thr
NM_201596.3:c.1619A>C (CACNB2) MANE Select	NP_963890.2:p.Asn540Thr
NM_201597.3:c.1547A>C (CACNB2)	NP_963891.1:p.Asn516Thr