Canonical Allele Identifier: CA411377278
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960775G>C (hg19) chr22:g.36564728G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564728G>C , CM000684.2:g.36564728G>C GRCh38
NC_000022.10:g.36960775G>C , CM000684.1:g.36960775G>C GRCh37
NC_000022.9:g.35290721G>C NCBI36
NG_031861.1:g.142916C>G
NG_031861.2:g.143131C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.595C>G MANE Select ENSP00000300105.6:p.His199Asp
ENST00000300105.6:c.595C>G ENSP00000300105.6:p.His199Asp
NM_006078.3:c.595C>G NP_006069.1:p.His199Asp
NM_006078.4:c.595C>G NP_006069.1:p.His199Asp
XM_017028531.2:c.337C>G XP_016884020.1:p.His113Asp
NM_001379051.1:c.526C>G NP_001365980.1:p.His176Asp
NM_006078.5:c.595C>G MANE Select NP_006069.1:p.His199Asp
NR_166440.1:n.1961C>G
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