Canonical Allele Identifier: CA185773130
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs964212490
MyVariant Identifiers: chr8:g.128717969A>T (hg19) chr8:g.127705724A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705724A>T , CM000670.2:g.127705724A>T GRCh38
NC_000008.10:g.128717969A>T , CM000670.1:g.128717969A>T GRCh37
NC_000008.9:g.128787151A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2481T>A
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Search 100 bp 3'