Canonical Allele Identifier: CA310097903
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs995018868
gnomAD v2: 19-54481161-T-A
gnomAD v3: 19-53977907-T-A
gnomAD v4: 19-53977907-T-A
MyVariant Identifiers: chr19:g.54481161T>A (hg19) chr19:g.53977907T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977907T>A , CM000681.2:g.53977907T>A GRCh38
NC_000019.9:g.54481161T>A , CM000681.1:g.54481161T>A GRCh37
NC_000019.8:g.59172973T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270458.4:c.284-239T>A MANE Select ENSP00000270458.3:n.284-239T>A
ENST00000270458.2:c.284-239T>A ENSP00000270458.2:n.284-239T>A
NM_031895.5:c.284-239T>A NP_114101.4:n.284-239T>A
NM_031895.6:c.284-239T>A MANE Select NP_114101.4:n.284-239T>A
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