Canonical Allele Identifier: CA847191344
Gene: CASC11 HGNC NCBI

Linked Data

dbSNP Id: rs1425832111
gnomAD v3: 8-127707588-A-G
gnomAD v4: 8-127707588-A-G
MyVariant Identifiers: chr8:g.128719833A>G (hg19) chr8:g.127707588A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127707588A>G , CM000670.2:g.127707588A>G GRCh38
NC_000008.10:g.128719833A>G , CM000670.1:g.128719833A>G GRCh37
NC_000008.9:g.128789015A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_117102.1:n.366-4345T>C
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