Canonical Allele Identifier: CA2245423477
Gene: C17orf100 HGNC NCBI

Linked Data

dbSNP Id: rs1972899375
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6656468C>T , CM000679.2:g.6656468C>T GRCh38
NC_000017.10:g.6559787C>T , CM000679.1:g.6559787C>T GRCh37
NC_000017.9:g.6500511C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000634977.1:n.431+3874C>T
ENST00000635042.1:n.724+3874C>T
Search 100 bp 5'
Search 100 bp 3'