Canonical Allele Identifier: CA1119137297

Gene: CCDC26

Linked Data

• dbSNP Id: rs1820171903
• gnomAD v3: 8-129465546-TC-T
• gnomAD v4: 8-129465546-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129465547del , CM000670.2:g.129465547del	GRCh38
NC_000008.10:g.130477793del , CM000670.1:g.130477793del	GRCh37
NC_000008.9:g.130546975del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.360+15096del
NR_130918.1:n.138-95170del
NR_130919.1:n.138-65863del
NR_130920.1:n.138-65863del