Canonical Allele Identifier: CA2245423507
Gene: C17orf100 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656487A= , CM000679.2:g.6656487A= GRCh38
NC_000017.10:g.6559806A= , CM000679.1:g.6559806A= GRCh37
NC_000017.9:g.6500530A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3893A=
ENST00000635042.1:n.724+3893A=