Canonical Allele Identifier: CA2245423488
Gene: C17orf100 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3877T=
ENST00000635042.1:n.724+3877T=