Canonical Allele Identifier: CA2342626706
Gene: CACNG8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977823C= , CM000681.2:g.53977823C= GRCh38
NC_000019.9:g.54481077C= , CM000681.1:g.54481077C= GRCh37
NC_000019.8:g.59172889C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270458.4:c.284-323C= MANE Select ENSP00000270458.3:n.284-323C=
ENST00000270458.2:c.284-323C= ENSP00000270458.2:n.284-323C=
NM_031895.5:c.284-323C= NP_114101.4:n.284-323C=
NM_031895.6:c.284-323C= MANE Select NP_114101.4:n.284-323C=