Canonical Allele Identifier: CA1119016790
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1178274587
gnomAD v3: 8-127705854-A-AT
gnomAD v4: 8-127705854-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705862dup , CM000670.2:g.127705862dup GRCh38
NC_000008.10:g.128718107dup , CM000670.1:g.128718107dup GRCh37
NC_000008.9:g.128787289dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2612dup
Search 100 bp 5'
Search 100 bp 3'