Canonical Allele Identifier: CA981120888

Gene: C17orf100

Linked Data

• dbSNP Id: rs1972899469
• gnomAD v3: 17-6656473-T-C
• gnomAD v4: 17-6656473-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6656473T>C , CM000679.2:g.6656473T>C	GRCh38
NC_000017.10:g.6559792T>C , CM000679.1:g.6559792T>C	GRCh37
NC_000017.9:g.6500516T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000634977.1:n.431+3879T>C
ENST00000635042.1:n.724+3879T>C