Canonical Allele Identifier: CA2245423597
Gene: C17orf100 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656548G= , CM000679.2:g.6656548G= GRCh38
NC_000017.10:g.6559867G= , CM000679.1:g.6559867G= GRCh37
NC_000017.9:g.6500591G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3954G=
ENST00000635042.1:n.724+3954G=