Canonical Allele Identifier: CA10212153

Gene: CACNG2

Linked Data

• dbSNP Id: rs760100050
• ExAC: 22:36960907 C / T
• gnomAD v4: 22-36564860-C-T
• MyVariant Identifiers: chr22:g.36960907C>T (hg19) ; chr22:g.36564860C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564860C>T , CM000684.2:g.36564860C>T	GRCh38
NC_000022.10:g.36960907C>T , CM000684.1:g.36960907C>T	GRCh37
NC_000022.9:g.35290853C>T	NCBI36
NG_031861.1:g.142784G>A
NG_031861.2:g.142999G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.463G>A MANE Select	ENSP00000300105.6:p.Val155Met
ENST00000300105.6:c.463G>A	ENSP00000300105.6:p.Val155Met
NM_006078.3:c.463G>A	NP_006069.1:p.Val155Met
NM_006078.4:c.463G>A	NP_006069.1:p.Val155Met
XM_017028531.2:c.205G>A	XP_016884020.1:p.Val69Met
NM_001379051.1:c.394G>A	NP_001365980.1:p.Val132Met
NM_006078.5:c.463G>A MANE Select	NP_006069.1:p.Val155Met
NR_166440.1:n.1829G>A