Canonical Allele Identifier: CA997100481
Gene: CACNG8 HGNC NCBI

Linked Data

dbSNP Id: rs2069339629
gnomAD v3: 19-53977931-T-G
gnomAD v4: 19-53977931-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977931T>G , CM000681.2:g.53977931T>G GRCh38
NC_000019.9:g.54481185T>G , CM000681.1:g.54481185T>G GRCh37
NC_000019.8:g.59172997T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270458.4:c.284-215T>G MANE Select ENSP00000270458.3:n.284-215T>G
ENST00000270458.2:c.284-215T>G ENSP00000270458.2:n.284-215T>G
NM_031895.5:c.284-215T>G NP_114101.4:n.284-215T>G
NM_031895.6:c.284-215T>G MANE Select NP_114101.4:n.284-215T>G
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