Canonical Allele Identifier: CA847190456
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1483140829
MyVariant Identifiers: chr8:g.128718228T>C (hg19) chr8:g.127705983T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705983T>C , CM000670.2:g.127705983T>C GRCh38
NC_000008.10:g.128718228T>C , CM000670.1:g.128718228T>C GRCh37
NC_000008.9:g.128787410T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2740A>G
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