Canonical Allele Identifier: CA752883892
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs983329412
gnomAD v3: 22-36701438-G-T
gnomAD v4: 22-36701438-G-T
MyVariant Identifiers: chr22:g.37097483G>T (hg19) chr22:g.36701438G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701438G>T , CM000684.2:g.36701438G>T GRCh38
NC_000022.10:g.37097483G>T , CM000684.1:g.37097483G>T GRCh37
NC_000022.9:g.35427429G>T NCBI36
NG_031861.1:g.6208C>A
NG_031861.2:g.6421C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.211+928C>A MANE Select ENSP00000300105.6:n.211+928C>A
ENST00000300105.6:c.211+928C>A ENSP00000300105.6:n.211+928C>A
NM_006078.3:c.211+928C>A NP_006069.1:n.211+928C>A
NM_006078.4:c.211+928C>A NP_006069.1:n.211+928C>A
NM_001379051.1:c.142+928C>A NP_001365980.1:n.142+928C>A
NM_006078.5:c.211+928C>A MANE Select NP_006069.1:n.211+928C>A
NR_166440.1:n.1387+928C>A
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