Canonical Allele Identifier: CA981120958
Gene: C17orf100 HGNC NCBI

Linked Data

gnomAD v3: 17-6656564-A-C
gnomAD v4: 17-6656564-A-C

Genomic Alleles

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

Transcript Alleles

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