Canonical Allele Identifier: CA185773117
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1029276020
MyVariant Identifiers: chr8:g.128717878C>A (hg19) chr8:g.127705633C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705633C>A , CM000670.2:g.127705633C>A GRCh38
NC_000008.10:g.128717878C>A , CM000670.1:g.128717878C>A GRCh37
NC_000008.9:g.128787060C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-2390G>T
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