Canonical Allele Identifier: CA985983219
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1907982227
gnomAD v3: 17-71112389-T-C
gnomAD v4: 17-71112389-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71112389T>C , CM000679.2:g.71112389T>C GRCh38
NC_000017.10:g.69108530T>C , CM000679.1:g.69108530T>C GRCh37
NC_000017.9:g.66620125T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104152.1:n.218-12771A>G
Search 100 bp 5'
Search 100 bp 3'