Canonical Allele Identifier: CA411377980
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960862T>C (hg19) chr22:g.36564815T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564815T>C , CM000684.2:g.36564815T>C GRCh38
NC_000022.10:g.36960862T>C , CM000684.1:g.36960862T>C GRCh37
NC_000022.9:g.35290808T>C NCBI36
NG_031861.1:g.142829A>G
NG_031861.2:g.143044A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.508A>G MANE Select ENSP00000300105.6:p.Lys170Glu
ENST00000300105.6:c.508A>G ENSP00000300105.6:p.Lys170Glu
NM_006078.3:c.508A>G NP_006069.1:p.Lys170Glu
NM_006078.4:c.508A>G NP_006069.1:p.Lys170Glu
XM_017028531.2:c.250A>G XP_016884020.1:p.Lys84Glu
NM_001379051.1:c.439A>G NP_001365980.1:p.Lys147Glu
NM_006078.5:c.508A>G MANE Select NP_006069.1:p.Lys170Glu
NR_166440.1:n.1874A>G
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