Canonical Allele Identifier: CA752858021

Gene: CACNG2

Linked Data

• dbSNP Id: rs1474883978
• gnomAD v4: 22-36564915-G-C
• MyVariant Identifiers: chr22:g.36960962G>C (hg19) ; chr22:g.36564915G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564915G>C , CM000684.2:g.36564915G>C	GRCh38
NC_000022.10:g.36960962G>C , CM000684.1:g.36960962G>C	GRCh37
NC_000022.9:g.35290908G>C	NCBI36
NG_031861.1:g.142729C>G
NG_031861.2:g.142944C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-29C>G MANE Select	ENSP00000300105.6:n.437-29C>G
ENST00000300105.6:c.437-29C>G	ENSP00000300105.6:n.437-29C>G
NM_006078.3:c.437-29C>G	NP_006069.1:n.437-29C>G
NM_006078.4:c.437-29C>G	NP_006069.1:n.437-29C>G
XM_017028531.2:c.179-29C>G	XP_016884020.1:n.179-29C>G
NM_001379051.1:c.368-29C>G	NP_001365980.1:n.368-29C>G
NM_006078.5:c.437-29C>G MANE Select	NP_006069.1:n.437-29C>G
NR_166440.1:n.1803-29C>G