Canonical Allele Identifier: CA376071802

Gene: CACNB2 NSUN6

Linked Data

• MyVariant Identifiers: chr10:g.18828370A>T (hg19) ; chr10:g.18539441A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.18539441A>T , CM000672.2:g.18539441A>T	GRCh38
NC_000010.10:g.18828370A>T , CM000672.1:g.18828370A>T	GRCh37
NC_000010.9:g.18868376A>T	NCBI36
NG_016195.1:g.403765A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377315.6:c.1556A>T (CACNB2)	ENSP00000366532.4:p.Tyr519Phe
ENST00000377319.9:c.1421A>T (CACNB2)	ENSP00000366536.3:p.Tyr474Phe
ENST00000645287.2:c.1544A>T (CACNB2)	ENSP00000496203.1:p.Tyr515Phe
ENST00000282343.13:c.1616A>T (CACNB2)	ENSP00000282343.8:p.Tyr539Phe
ENST00000324631.13:c.1700A>T (CACNB2) MANE Select	ENSP00000320025.8:p.Tyr567Phe
ENST00000377315.5:c.1556A>T (CACNB2)	ENSP00000366532.4:p.Tyr519Phe
ENST00000377319.8:c.1421A>T (CACNB2)	ENSP00000366536.3:p.Tyr474Phe
ENST00000377329.10:c.1538A>T (CACNB2) MANE Plus Clinical	ENSP00000366546.4:p.Tyr513Phe
ENST00000377331.8:c.1325A>T (CACNB2)	ENSP00000366548.4:p.Tyr442Phe
ENST00000643096.2:c.1502A>T (CACNB2)	ENSP00000494209.2:p.Tyr501Phe
ENST00000645287.1:c.1544A>T (CACNB2)	ENSP00000496203.1:p.Tyr515Phe
ENST00000647168.2:c.*841A>T (CACNB2)	ENSP00000495854.2:n.*841A>T
ENST00000650685.1:c.1442A>T (CACNB2)	ENSP00000498460.1:p.Tyr481Phe
ENST00000651330.1:c.*974A>T (CACNB2)	ENSP00000498457.1:n.*974A>T
ENST00000651468.1:c.1257A>T (CACNB2)	ENSP00000498352.1:n.1257A>T
ENST00000651928.1:c.*939A>T (CACNB2)	ENSP00000499177.1:n.*939A>T
ENST00000652391.1:c.1520A>T (CACNB2)	ENSP00000498938.1:p.Tyr507Phe
ENST00000652478.1:c.*800A>T (CACNB2)	ENSP00000498812.1:n.*800A>T
ENST00000282343.12:c.1616A>T (CACNB2)	ENSP00000282343.8:p.Tyr539Phe
ENST00000324631.11:c.1700A>T (CACNB2)	ENSP00000320025.7:p.Tyr567Phe
ENST00000352115.10:c.1628A>T (CACNB2)	ENSP00000344474.6:p.Tyr543Phe
ENST00000377315.4:c.1556A>T (CACNB2)	ENSP00000366532.4:p.Tyr519Phe
ENST00000377319.7:c.1421A>T (CACNB2)	ENSP00000366536.3:p.Tyr474Phe
ENST00000377328.5:c.950A>T (CACNB2)	ENSP00000366545.1:p.Tyr317Phe
ENST00000377329.8:c.1538A>T (CACNB2)	ENSP00000366546.4:p.Tyr513Phe
ENST00000377331.6:c.1544A>T (CACNB2)	ENSP00000366548.2:p.Tyr515Phe
ENST00000396576.6:c.1535A>T (CACNB2)	ENSP00000379821.2:p.Tyr512Phe
ENST00000612134.4:c.1404A>T (CACNB2)	ENSP00000480563.1:n.1404A>T
ENST00000612743.1:c.212A>T (CACNB2)	ENSP00000478676.1:p.Tyr71Phe
ENST00000615785.4:c.785A>T (CACNB2)	ENSP00000480260.1:p.Tyr262Phe
ENST00000617363.4:c.1463A>T (CACNB2)	ENSP00000479756.1:p.Tyr488Phe
NM_000724.3:c.1535A>T (CACNB2)	NP_000715.2:p.Tyr512Phe
NM_001167945.1:c.1502A>T (CACNB2)	NP_001161417.1:p.Tyr501Phe
NM_201570.2:c.1556A>T (CACNB2)	NP_963864.1:p.Tyr519Phe
NM_201571.3:c.1616A>T (CACNB2)	NP_963865.2:p.Tyr539Phe
NM_201572.3:c.1544A>T (CACNB2)	NP_963866.2:p.Tyr515Phe
NM_201590.2:c.1538A>T (CACNB2)	NP_963884.2:p.Tyr513Phe
NM_201593.2:c.1586A>T (CACNB2)	NP_963887.2:p.Tyr529Phe
NM_201596.2:c.1700A>T (CACNB2)	NP_963890.2:p.Tyr567Phe
NM_201597.2:c.1628A>T (CACNB2)	NP_963891.1:p.Tyr543Phe
XM_005252588.2:c.1442A>T (CACNB2)	XP_005252645.1:p.Tyr481Phe
XM_005252591.2:c.860A>T (CACNB2)	XP_005252648.1:p.Tyr287Phe
XM_006717502.2:c.1520A>T (CACNB2)	XP_006717565.1:p.Tyr507Phe
XM_011519659.1:c.1466A>T (CACNB2)	XP_011517961.1:p.Tyr489Phe
XM_011519660.1:c.1421A>T (CACNB2)	XP_011517962.1:p.Tyr474Phe
NM_001330060.1:c.1421A>T (CACNB2)	NP_001316989.1:p.Tyr474Phe
XM_005252588.4:c.1442A>T (CACNB2)	XP_005252645.1:p.Tyr481Phe
XM_005252591.3:c.860A>T (CACNB2)	XP_005252648.1:p.Tyr287Phe
XM_006717502.3:c.1520A>T (CACNB2)	XP_006717565.1:p.Tyr507Phe
XM_011519659.2:c.1466A>T (CACNB2)	XP_011517961.1:p.Tyr489Phe
XM_017016625.1:c.860A>T (CACNB2)	XP_016872114.1:p.Tyr287Phe
XR_001747060.1:n.2423+2628T>A (NSUN6)
XR_001747198.1:n.1825A>T (CACNB2)
NM_000724.4:c.1535A>T (CACNB2)	NP_000715.2:p.Tyr512Phe
NM_001167945.2:c.1502A>T (CACNB2)	NP_001161417.1:p.Tyr501Phe
NM_001330060.2:c.1421A>T (CACNB2)	NP_001316989.1:p.Tyr474Phe
NM_201570.3:c.1556A>T (CACNB2)	NP_963864.1:p.Tyr519Phe
NM_201571.4:c.1616A>T (CACNB2)	NP_963865.2:p.Tyr539Phe
NM_201572.4:c.1544A>T (CACNB2)	NP_963866.2:p.Tyr515Phe
NM_201590.3:c.1538A>T (CACNB2) MANE Plus Clinical	NP_963884.2:p.Tyr513Phe
NM_201593.3:c.1586A>T (CACNB2)	NP_963887.2:p.Tyr529Phe
NM_201596.3:c.1700A>T (CACNB2) MANE Select	NP_963890.2:p.Tyr567Phe
NM_201597.3:c.1628A>T (CACNB2)	NP_963891.1:p.Tyr543Phe