Canonical Allele Identifier: CA185773139
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs894973801
MyVariant Identifiers: chr8:g.128718064A>G (hg19) chr8:g.127705819A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705819A>G , CM000670.2:g.127705819A>G GRCh38
NC_000008.10:g.128718064A>G , CM000670.1:g.128718064A>G GRCh37
NC_000008.9:g.128787246A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_117102.1:n.366-2576T>C
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