Canonical Allele Identifier: CA2245423513
Gene: C17orf100 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656490C= , CM000679.2:g.6656490C= GRCh38
NC_000017.10:g.6559809C= , CM000679.1:g.6559809C= GRCh37
NC_000017.9:g.6500533C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3896C=
ENST00000635042.1:n.724+3896C=