Canonical Allele Identifier: CA774185233
Gene: C17orf100 HGNC NCBI

Linked Data

dbSNP Id: rs1396093064
gnomAD v3: 17-6656546-A-G
gnomAD v4: 17-6656546-A-G
MyVariant Identifiers: chr17:g.6559865A>G (hg19) chr17:g.6656546A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656546A>G , CM000679.2:g.6656546A>G GRCh38
NC_000017.10:g.6559865A>G , CM000679.1:g.6559865A>G GRCh37
NC_000017.9:g.6500589A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3952A>G
ENST00000635042.1:n.724+3952A>G
Search 100 bp 5'
Search 100 bp 3'