Canonical Allele Identifier: CA10212128
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs769458037
ExAC: 22:36960728 G / C
gnomAD v2: 22-36960728-G-C
gnomAD v3: 22-36564681-G-C
gnomAD v4: 22-36564681-G-C
MyVariant Identifiers: chr22:g.36960728G>C (hg19) chr22:g.36564681G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564681G>C , CM000684.2:g.36564681G>C GRCh38
NC_000022.10:g.36960728G>C , CM000684.1:g.36960728G>C GRCh37
NC_000022.9:g.35290674G>C NCBI36
NG_031861.1:g.142963C>G
NG_031861.2:g.143178C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.642C>G MANE Select ENSP00000300105.6:p.Ala214=
ENST00000300105.6:c.642C>G ENSP00000300105.6:p.Ala214=
NM_006078.3:c.642C>G NP_006069.1:p.Ala214=
NM_006078.4:c.642C>G NP_006069.1:p.Ala214=
XM_017028531.2:c.384C>G XP_016884020.1:p.Ala128=
NM_001379051.1:c.573C>G NP_001365980.1:p.Ala191=
NM_006078.5:c.642C>G MANE Select NP_006069.1:p.Ala214=
NR_166440.1:n.2008C>G
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