Canonical Allele Identifier: CA1119016713
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1815453092
gnomAD v3: 8-127705655-G-A
gnomAD v4: 8-127705655-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127705655G>A , CM000670.2:g.127705655G>A GRCh38
NC_000008.10:g.128717900G>A , CM000670.1:g.128717900G>A GRCh37
NC_000008.9:g.128787082G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-2412C>T
Search 100 bp 5'
Search 100 bp 3'