Canonical Allele Identifier: CA847166741
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1187379586
MyVariant Identifiers: chr8:g.128484907C>T (hg19) chr8:g.127472662C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472662C>T , CM000670.2:g.127472662C>T GRCh38
NC_000008.10:g.128484907C>T , CM000670.1:g.128484907C>T GRCh37
NC_000008.9:g.128554089C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+6421G>A
NR_117100.1:n.1041+6421G>A
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