Canonical Allele Identifier: CA985992377
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs1908471756
gnomAD v3: 17-71129471-T-C
gnomAD v4: 17-71129471-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129471T>C , CM000679.2:g.71129471T>C GRCh38
NC_000017.10:g.69125612T>C , CM000679.1:g.69125612T>C GRCh37
NC_000017.9:g.66637207T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+2919A>G
Search 100 bp 5'
Search 100 bp 3'