Canonical Allele Identifier: CA981120897

Gene: C17orf100

Linked Data

• dbSNP Id: rs1597638652
• gnomAD v3: 17-6656489-A-T
• gnomAD v4: 17-6656489-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.6656489A>T , CM000679.2:g.6656489A>T	GRCh38
NC_000017.10:g.6559808A>T , CM000679.1:g.6559808A>T	GRCh37
NC_000017.9:g.6500532A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000634977.1:n.431+3895A>T
ENST00000635042.1:n.724+3895A>T