Canonical Allele Identifier: CA624669629
Gene: C17orf100 HGNC NCBI

Linked Data

dbSNP Id: rs1196120271
gnomAD v2: 17-6559790-T-A
gnomAD v3: 17-6656471-T-A
gnomAD v4: 17-6656471-T-A
MyVariant Identifiers: chr17:g.6559790T>A (hg19) chr17:g.6656471T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656471T>A , CM000679.2:g.6656471T>A GRCh38
NC_000017.10:g.6559790T>A , CM000679.1:g.6559790T>A GRCh37
NC_000017.9:g.6500514T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3877T>A
ENST00000635042.1:n.724+3877T>A
Search 100 bp 5'
Search 100 bp 3'