Canonical Allele Identifier: CA2342626697
Gene: CACNG8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977811C= , CM000681.2:g.53977811C= GRCh38
NC_000019.9:g.54481065C= , CM000681.1:g.54481065C= GRCh37
NC_000019.8:g.59172877C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270458.4:c.284-335C= MANE Select ENSP00000270458.3:n.284-335C=
ENST00000270458.2:c.284-335C= ENSP00000270458.2:n.284-335C=
NM_031895.5:c.284-335C= NP_114101.4:n.284-335C=
NM_031895.6:c.284-335C= MANE Select NP_114101.4:n.284-335C=
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