Canonical Allele Identifier: CA411376847
Gene: CACNG2 HGNC NCBI

Linked Data

gnomAD v4: 22-36564667-T-C
MyVariant Identifiers: chr22:g.36960714T>C (hg19) chr22:g.36564667T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564667T>C , CM000684.2:g.36564667T>C GRCh38
NC_000022.10:g.36960714T>C , CM000684.1:g.36960714T>C GRCh37
NC_000022.9:g.35290660T>C NCBI36
NG_031861.1:g.142977A>G
NG_031861.2:g.143192A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.656A>G MANE Select ENSP00000300105.6:p.Gln219Arg
ENST00000300105.6:c.656A>G ENSP00000300105.6:p.Gln219Arg
NM_006078.3:c.656A>G NP_006069.1:p.Gln219Arg
NM_006078.4:c.656A>G NP_006069.1:p.Gln219Arg
XM_017028531.2:c.398A>G XP_016884020.1:p.Gln133Arg
NM_001379051.1:c.587A>G NP_001365980.1:p.Gln196Arg
NM_006078.5:c.656A>G MANE Select NP_006069.1:p.Gln219Arg
NR_166440.1:n.2022A>G
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