Canonical Allele Identifier: CA10212156
Gene: CACNG2 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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