Canonical Allele Identifier: CA2245423620
Gene: C17orf100 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656564A= , CM000679.2:g.6656564A= GRCh38
NC_000017.10:g.6559883A= , CM000679.1:g.6559883A= GRCh37
NC_000017.9:g.6500607A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3970A=
ENST00000635042.1:n.724+3970A=