Canonical Allele Identifier: CA2566748436
Gene: C17orf100 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656590G>C , CM000679.2:g.6656590G>C GRCh38
NC_000017.10:g.6559909G>C , CM000679.1:g.6559909G>C GRCh37
NC_000017.9:g.6500633G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3996G>C
ENST00000635042.1:n.724+3996G>C