Canonical Allele Identifier: CA186000947
Gene: CCDC26 HGNC NCBI
dbSNP:
10098310
gnomAD v2:
8:130613614 G / A
gnomAD v3:
8:129601368 G / A
gnomAD v4:
chr8-129601368-G-A
Joint Max Group AF 0.64263427 (SAS)
Genomes Max Group AF 0.64263427 (SAS)
MyVariant.info:
GRCh38 chr8:g.129601368G>A
GRCh37 chr8:g.130613614G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601368G>A , CM000670.2:g.129601368G>A GRCh38
NC_000008.10:g.130613614G>A , CM000670.1:g.130613614G>A GRCh37
NC_000008.9:g.130682796G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78560C>T
Search 100 bp 5'
Search 100 bp 3'