Canonical Allele Identifier: CA411377527
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960813G>T (hg19) chr22:g.36564766G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564766G>T , CM000684.2:g.36564766G>T GRCh38
NC_000022.10:g.36960813G>T , CM000684.1:g.36960813G>T GRCh37
NC_000022.9:g.35290759G>T NCBI36
NG_031861.1:g.142878C>A
NG_031861.2:g.143093C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.557C>A MANE Select ENSP00000300105.6:p.Ser186Tyr
ENST00000300105.6:c.557C>A ENSP00000300105.6:p.Ser186Tyr
NM_006078.3:c.557C>A NP_006069.1:p.Ser186Tyr
NM_006078.4:c.557C>A NP_006069.1:p.Ser186Tyr
XM_017028531.2:c.299C>A XP_016884020.1:p.Ser100Tyr
NM_001379051.1:c.488C>A NP_001365980.1:p.Ser163Tyr
NM_006078.5:c.557C>A MANE Select NP_006069.1:p.Ser186Tyr
NR_166440.1:n.1923C>A
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