Canonical Allele Identifier: CA2590188692
Gene: CACNG2 HGNC NCBI

Linked Data

dbSNP Id: rs2146023462
gnomAD v3: 22-36701424-C-A
gnomAD v4: 22-36701424-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36701424C>A , CM000684.2:g.36701424C>A GRCh38
NC_000022.10:g.37097469C>A , CM000684.1:g.37097469C>A GRCh37
NC_000022.9:g.35427415C>A NCBI36
NG_031861.1:g.6222G>T
NG_031861.2:g.6435G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.211+942G>T MANE Select ENSP00000300105.6:n.211+942G>T
ENST00000300105.6:c.211+942G>T ENSP00000300105.6:n.211+942G>T
NM_006078.3:c.211+942G>T NP_006069.1:n.211+942G>T
NM_006078.4:c.211+942G>T NP_006069.1:n.211+942G>T
NM_001379051.1:c.142+942G>T NP_001365980.1:n.142+942G>T
NM_006078.5:c.211+942G>T MANE Select NP_006069.1:n.211+942G>T
NR_166440.1:n.1387+942G>T
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