Canonical Allele Identifier: CA411376365
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960669T>C (hg19) chr22:g.36564622T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564622T>C , CM000684.2:g.36564622T>C GRCh38
NC_000022.10:g.36960669T>C , CM000684.1:g.36960669T>C GRCh37
NC_000022.9:g.35290615T>C NCBI36
NG_031861.1:g.143022A>G
NG_031861.2:g.143237A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.701A>G MANE Select ENSP00000300105.6:p.Gln234Arg
ENST00000300105.6:c.701A>G ENSP00000300105.6:p.Gln234Arg
NM_006078.3:c.701A>G NP_006069.1:p.Gln234Arg
NM_006078.4:c.701A>G NP_006069.1:p.Gln234Arg
XM_017028531.2:c.443A>G XP_016884020.1:p.Gln148Arg
NM_001379051.1:c.632A>G NP_001365980.1:p.Gln211Arg
NM_006078.5:c.701A>G MANE Select NP_006069.1:p.Gln234Arg
NR_166440.1:n.2067A>G
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