Canonical Allele Identifier: CA2342626718
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs2069339073
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977853C>A , CM000681.2:g.53977853C>A GRCh38
NC_000019.9:g.54481107C>A , CM000681.1:g.54481107C>A GRCh37
NC_000019.8:g.59172919C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270458.4:c.284-293C>A MANE Select ENSP00000270458.3:n.284-293C>A
ENST00000270458.2:c.284-293C>A ENSP00000270458.2:n.284-293C>A
NM_031895.5:c.284-293C>A NP_114101.4:n.284-293C>A
NM_031895.6:c.284-293C>A MANE Select NP_114101.4:n.284-293C>A
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