Canonical Allele Identifier: CA847191334
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1403324861
gnomAD v3: 8-127707555-CT-C
gnomAD v4: 8-127707555-CT-C
MyVariant Identifiers: chr8:g.128719801del (hg19) chr8:g.127707556del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707556del , CM000670.2:g.127707556del GRCh38
NC_000008.10:g.128719801del , CM000670.1:g.128719801del GRCh37
NC_000008.9:g.128788983del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4313del
Search 100 bp 5'
Search 100 bp 3'