Canonical Allele Identifier: CA2656451706
Gene: CACNG2 HGNC NCBI

Linked Data

gnomAD v4: 22-36564981-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564981G>A , CM000684.2:g.36564981G>A GRCh38
NC_000022.10:g.36961028G>A , CM000684.1:g.36961028G>A GRCh37
NC_000022.9:g.35290974G>A NCBI36
NG_031861.1:g.142663C>T
NG_031861.2:g.142878C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.437-95C>T MANE Select ENSP00000300105.6:n.437-95C>T
ENST00000300105.6:c.437-95C>T ENSP00000300105.6:n.437-95C>T
NM_006078.3:c.437-95C>T NP_006069.1:n.437-95C>T
NM_006078.4:c.437-95C>T NP_006069.1:n.437-95C>T
XM_017028531.2:c.179-95C>T XP_016884020.1:n.179-95C>T
NM_001379051.1:c.368-95C>T NP_001365980.1:n.368-95C>T
NM_006078.5:c.437-95C>T MANE Select NP_006069.1:n.437-95C>T
NR_166440.1:n.1803-95C>T
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