Canonical Allele Identifier: CA185996162

Gene: CCDC26

Linked Data

• dbSNP Id: rs570547929
• gnomAD v3: 8-129559932-T-C
• gnomAD v4: 8-129559932-T-C
• MyVariant Identifiers: chr8:g.130572178T>C (hg19) ; chr8:g.129559932T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559932T>C , CM000670.2:g.129559932T>C	GRCh38
NC_000008.10:g.130572178T>C , CM000670.1:g.130572178T>C	GRCh37
NC_000008.9:g.130641360T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79242A>G
NR_130918.1:n.137+14950A>G
NR_130919.1:n.137+14950A>G
NR_130920.1:n.137+14950A>G