Canonical Allele Identifier: CA847190226
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1328578381
MyVariant Identifiers: chr8:g.128717805C>T (hg19) chr8:g.127705560C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705560C>T , CM000670.2:g.127705560C>T GRCh38
NC_000008.10:g.128717805C>T , CM000670.1:g.128717805C>T GRCh37
NC_000008.9:g.128786987C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2317G>A
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