Canonical Allele Identifier: CA639392933
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs763253659
gnomAD v2: 22-36960937-C-T
gnomAD v3: 22-36564890-C-T
gnomAD v4: 22-36564890-C-T
MyVariant Identifiers: chr22:g.36960937C>T (hg19) chr22:g.36564890C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564890C>T , CM000684.2:g.36564890C>T GRCh38
NC_000022.10:g.36960937C>T , CM000684.1:g.36960937C>T GRCh37
NC_000022.9:g.35290883C>T NCBI36
NG_031861.1:g.142754G>A
NG_031861.2:g.142969G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-4G>A MANE Select ENSP00000300105.6:n.437-4G>A
ENST00000300105.6:c.437-4G>A ENSP00000300105.6:n.437-4G>A
NM_006078.3:c.437-4G>A NP_006069.1:n.437-4G>A
NM_006078.4:c.437-4G>A NP_006069.1:n.437-4G>A
XM_017028531.2:c.179-4G>A XP_016884020.1:n.179-4G>A
NM_001379051.1:c.368-4G>A NP_001365980.1:n.368-4G>A
NM_006078.5:c.437-4G>A MANE Select NP_006069.1:n.437-4G>A
NR_166440.1:n.1803-4G>A
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