Canonical Allele Identifier: CA883512807
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs1245790770
gnomAD v3: 19-53977826-G-T
gnomAD v4: 19-53977826-G-T
MyVariant Identifiers: chr19:g.54481080G>T (hg19) chr19:g.53977826G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977826G>T , CM000681.2:g.53977826G>T GRCh38
NC_000019.9:g.54481080G>T , CM000681.1:g.54481080G>T GRCh37
NC_000019.8:g.59172892G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270458.4:c.284-320G>T MANE Select ENSP00000270458.3:n.284-320G>T
ENST00000270458.2:c.284-320G>T ENSP00000270458.2:n.284-320G>T
NM_031895.5:c.284-320G>T NP_114101.4:n.284-320G>T
NM_031895.6:c.284-320G>T MANE Select NP_114101.4:n.284-320G>T
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