Canonical Allele Identifier: CA752858042

Gene: CACNG2

Linked Data

• dbSNP Id: rs1272252570
• gnomAD v4: 22-36564972-A-G
• MyVariant Identifiers: chr22:g.36961019A>G (hg19) ; chr22:g.36564972A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564972A>G , CM000684.2:g.36564972A>G	GRCh38
NC_000022.10:g.36961019A>G , CM000684.1:g.36961019A>G	GRCh37
NC_000022.9:g.35290965A>G	NCBI36
NG_031861.1:g.142672T>C
NG_031861.2:g.142887T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-86T>C MANE Select	ENSP00000300105.6:n.437-86T>C
ENST00000300105.6:c.437-86T>C	ENSP00000300105.6:n.437-86T>C
NM_006078.3:c.437-86T>C	NP_006069.1:n.437-86T>C
NM_006078.4:c.437-86T>C	NP_006069.1:n.437-86T>C
XM_017028531.2:c.179-86T>C	XP_016884020.1:n.179-86T>C
NM_001379051.1:c.368-86T>C	NP_001365980.1:n.368-86T>C
NM_006078.5:c.437-86T>C MANE Select	NP_006069.1:n.437-86T>C
NR_166440.1:n.1803-86T>C