Canonical Allele Identifier: CA847392915

Gene: CCDC26

Linked Data

• dbSNP Id: rs1366736409
• gnomAD v3: 8-129601273-T-G
• gnomAD v4: 8-129601273-T-G
• MyVariant Identifiers: chr8:g.130613519T>G (hg19) ; chr8:g.129601273T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601273T>G , CM000670.2:g.129601273T>G	GRCh38
NC_000008.10:g.130613519T>G , CM000670.1:g.130613519T>G	GRCh37
NC_000008.9:g.130682701T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_130917.1:n.312+78655A>C