Canonical Allele Identifier: CA1119164168

Gene: CCDC26

Linked Data

• dbSNP Id: rs2030288081
• gnomAD v3: 8-129601334-C-T
• gnomAD v4: 8-129601334-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601334C>T , CM000670.2:g.129601334C>T	GRCh38
NC_000008.10:g.130613580C>T , CM000670.1:g.130613580C>T	GRCh37
NC_000008.9:g.130682762C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78594G>A