Canonical Allele Identifier: CA883512847
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs1451269249
MyVariant Identifiers: chr19:g.54481157A>T (hg19) chr19:g.53977903A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977903A>T , CM000681.2:g.53977903A>T GRCh38
NC_000019.9:g.54481157A>T , CM000681.1:g.54481157A>T GRCh37
NC_000019.8:g.59172969A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270458.4:c.284-243A>T MANE Select ENSP00000270458.3:n.284-243A>T
ENST00000270458.2:c.284-243A>T ENSP00000270458.2:n.284-243A>T
NM_031895.5:c.284-243A>T NP_114101.4:n.284-243A>T
NM_031895.6:c.284-243A>T MANE Select NP_114101.4:n.284-243A>T
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