Canonical Allele Identifier: CA185745365
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs947612996
gnomAD v2: 8-128484916-A-C
gnomAD v3: 8-127472671-A-C
gnomAD v4: 8-127472671-A-C
MyVariant Identifiers: chr8:g.128484916A>C (hg19) chr8:g.127472671A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472671A>C , CM000670.2:g.127472671A>C GRCh38
NC_000008.10:g.128484916A>C , CM000670.1:g.128484916A>C GRCh37
NC_000008.9:g.128554098A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+6412T>G
NR_117100.1:n.1041+6412T>G
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