Canonical Allele Identifier: CA310097914
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs962637109
gnomAD v3: 19-53977935-C-A
gnomAD v4: 19-53977935-C-A
MyVariant Identifiers: chr19:g.54481189C>A (hg19) chr19:g.53977935C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977935C>A , CM000681.2:g.53977935C>A GRCh38
NC_000019.9:g.54481189C>A , CM000681.1:g.54481189C>A GRCh37
NC_000019.8:g.59173001C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270458.4:c.284-211C>A MANE Select ENSP00000270458.3:n.284-211C>A
ENST00000270458.2:c.284-211C>A ENSP00000270458.2:n.284-211C>A
NM_031895.5:c.284-211C>A NP_114101.4:n.284-211C>A
NM_031895.6:c.284-211C>A MANE Select NP_114101.4:n.284-211C>A
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