Canonical Allele Identifier: CA323997924
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs111829699
gnomAD v2: 22-36960974-G-A
gnomAD v3: 22-36564927-G-A
gnomAD v4: 22-36564927-G-A
MyVariant Identifiers: chr22:g.36960974G>A (hg19) chr22:g.36564927G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564927G>A , CM000684.2:g.36564927G>A GRCh38
NC_000022.10:g.36960974G>A , CM000684.1:g.36960974G>A GRCh37
NC_000022.9:g.35290920G>A NCBI36
NG_031861.1:g.142717C>T
NG_031861.2:g.142932C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-41C>T MANE Select ENSP00000300105.6:n.437-41C>T
ENST00000300105.6:c.437-41C>T ENSP00000300105.6:n.437-41C>T
NM_006078.3:c.437-41C>T NP_006069.1:n.437-41C>T
NM_006078.4:c.437-41C>T NP_006069.1:n.437-41C>T
XM_017028531.2:c.179-41C>T XP_016884020.1:n.179-41C>T
NM_001379051.1:c.368-41C>T NP_001365980.1:n.368-41C>T
NM_006078.5:c.437-41C>T MANE Select NP_006069.1:n.437-41C>T
NR_166440.1:n.1803-41C>T
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