Canonical Allele Identifier: CA16575082

Gene: CACNG8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53977896T>C , CM000681.2:g.53977896T>C	GRCh38
NC_000019.9:g.54481150T>C , CM000681.1:g.54481150T>C	GRCh37
NC_000019.8:g.59172962T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270458.4:c.284-250T>C MANE Select	ENSP00000270458.3:n.284-250T>C
ENST00000270458.2:c.284-250T>C	ENSP00000270458.2:n.284-250T>C
NM_031895.5:c.284-250T>C	NP_114101.4:n.284-250T>C
NM_031895.6:c.284-250T>C MANE Select	NP_114101.4:n.284-250T>C