Canonical Allele Identifier: CA774185242
Gene: C17orf100 HGNC NCBI

Linked Data

dbSNP Id: rs1195430729
MyVariant Identifiers: chr17:g.6559899A>T (hg19) chr17:g.6656580A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656580A>T , CM000679.2:g.6656580A>T GRCh38
NC_000017.10:g.6559899A>T , CM000679.1:g.6559899A>T GRCh37
NC_000017.9:g.6500623A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3986A>T
ENST00000635042.1:n.724+3986A>T
Search 100 bp 5'
Search 100 bp 3'