Canonical Allele Identifier: CA2814833948

Gene: CACNG8

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53977821A>G , CM000681.2:g.53977821A>G	GRCh38
NC_000019.9:g.54481075A>G , CM000681.1:g.54481075A>G	GRCh37
NC_000019.8:g.59172887A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000270458.4:c.284-325A>G MANE Select	ENSP00000270458.3:n.284-325A>G
ENST00000270458.2:c.284-325A>G	ENSP00000270458.2:n.284-325A>G
NM_031895.5:c.284-325A>G	NP_114101.4:n.284-325A>G
NM_031895.6:c.284-325A>G MANE Select	NP_114101.4:n.284-325A>G