Canonical Allele Identifier: CA323997914

Gene: CACNG2

Linked Data

• dbSNP Id: rs183029332
• gnomAD v4: 22-36564910-T-G
• MyVariant Identifiers: chr22:g.36960957T>G (hg19) ; chr22:g.36564910T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564910T>G , CM000684.2:g.36564910T>G	GRCh38
NC_000022.10:g.36960957T>G , CM000684.1:g.36960957T>G	GRCh37
NC_000022.9:g.35290903T>G	NCBI36
NG_031861.1:g.142734A>C
NG_031861.2:g.142949A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.437-24A>C MANE Select	ENSP00000300105.6:n.437-24A>C
ENST00000300105.6:c.437-24A>C	ENSP00000300105.6:n.437-24A>C
NM_006078.3:c.437-24A>C	NP_006069.1:n.437-24A>C
NM_006078.4:c.437-24A>C	NP_006069.1:n.437-24A>C
XM_017028531.2:c.179-24A>C	XP_016884020.1:n.179-24A>C
NM_001379051.1:c.368-24A>C	NP_001365980.1:n.368-24A>C
NM_006078.5:c.437-24A>C MANE Select	NP_006069.1:n.437-24A>C
NR_166440.1:n.1803-24A>C