Canonical Allele Identifier: CA758941670

Gene: CACNB4

Linked Data

• dbSNP Id: rs1304978844
• gnomAD v4: 2-152098859-C-T
• MyVariant Identifiers: chr2:g.152955373C>T (hg19) ; chr2:g.152098859C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.152098859C>T , CM000664.2:g.152098859C>T	GRCh38
NC_000002.11:g.152955373C>T , CM000664.1:g.152955373C>T	GRCh37
NC_000002.10:g.152663619C>T	NCBI36
NG_012641.1:g.5221G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000201943.10:c.63+90G>A	ENSP00000201943.5:n.63+90G>A
ENST00000427385.6:c.63+90G>A	ENSP00000410978.2:n.63+90G>A
ENST00000470066.2:n.192+90G>A
ENST00000539935.7:c.63+90G>A MANE Select	ENSP00000438949.1:n.63+90G>A
ENST00000637309.1:c.63+90G>A	ENSP00000490127.1:n.63+90G>A
ENST00000201943.9:c.63+90G>A	ENSP00000201943.5:n.63+90G>A
ENST00000539935.5:c.63+90G>A	ENSP00000438949.1:n.63+90G>A
NM_000726.3:c.63+90G>A	NP_000717.2:n.63+90G>A
NM_001145798.1:c.63+90G>A	NP_001139270.1:n.63+90G>A
XM_011511797.1:c.63+90G>A	XP_011510099.1:n.63+90G>A
XM_011511798.1:c.63+90G>A	XP_011510100.1:n.63+90G>A
XM_011511799.1:c.63+90G>A	XP_011510101.1:n.63+90G>A
XR_923022.1:n.1040+90G>A
XR_923023.1:n.1040+90G>A
NM_000726.4:c.63+90G>A	NP_000717.2:n.63+90G>A
NM_001005746.3:c.-210G>A	NP_001005746.1:n.-210G>A
NM_001145798.2:c.63+90G>A	NP_001139270.1:n.63+90G>A
NM_001330113.1:c.-210G>A	NP_001317042.1:n.-210G>A
XM_011511797.3:c.63+90G>A	XP_011510099.1:n.63+90G>A
XR_002959337.1:n.216+90G>A
XR_923022.3:n.216+90G>A
NM_000726.5:c.63+90G>A MANE Select	NP_000717.2:n.63+90G>A