Canonical Allele Identifier: CA514475153
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960707A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564660A>C , CM000684.2:g.36564660A>C GRCh38
NC_000022.10:g.36960707A>C , CM000684.1:g.36960707A>C GRCh37
NC_000022.9:g.35290653A>C NCBI36
NG_031861.1:g.142984T>G
NG_031861.2:g.143199T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.663T>G MANE Select ENSP00000300105.6:p.Ser221=
ENST00000300105.6:c.663T>G ENSP00000300105.6:p.Ser221=
NM_006078.3:c.663T>G NP_006069.1:p.Ser221=
NM_006078.4:c.663T>G NP_006069.1:p.Ser221=
XM_017028531.2:c.405T>G XP_016884020.1:p.Ser135=
NM_001379051.1:c.594T>G NP_001365980.1:p.Ser198=
NM_006078.5:c.663T>G MANE Select NP_006069.1:p.Ser221=
NR_166440.1:n.2029T>G
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