Canonical Allele Identifier: CA585157954
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1186424929
gnomAD v2: 8-130572471-A-G
gnomAD v3: 8-129560225-A-G
gnomAD v4: 8-129560225-A-G
MyVariant Identifiers: chr8:g.130572471A>G (hg19) chr8:g.129560225A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560225A>G , CM000670.2:g.129560225A>G GRCh38
NC_000008.10:g.130572471A>G , CM000670.1:g.130572471A>G GRCh37
NC_000008.9:g.130641653A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79535T>C
NR_130918.1:n.137+14657T>C
NR_130919.1:n.137+14657T>C
NR_130920.1:n.137+14657T>C
Search 100 bp 5'
Search 100 bp 3'