Canonical Allele Identifier: CA981120895
Gene: C17orf100 HGNC NCBI

Linked Data

dbSNP Id: rs1972899527
gnomAD v3: 17-6656481-C-G
gnomAD v4: 17-6656481-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656481C>G , CM000679.2:g.6656481C>G GRCh38
NC_000017.10:g.6559800C>G , CM000679.1:g.6559800C>G GRCh37
NC_000017.9:g.6500524C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3887C>G
ENST00000635042.1:n.724+3887C>G
Search 100 bp 5'
Search 100 bp 3'