Canonical Allele Identifier: CA185996195
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs116329408
gnomAD v2: 8-130572437-A-G
gnomAD v3: 8-129560191-A-G
gnomAD v4: 8-129560191-A-G
MyVariant Identifiers: chr8:g.130572437A>G (hg19) chr8:g.129560191A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560191A>G , CM000670.2:g.129560191A>G GRCh38
NC_000008.10:g.130572437A>G , CM000670.1:g.130572437A>G GRCh37
NC_000008.9:g.130641619A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79501T>C
NR_130918.1:n.137+14691T>C
NR_130919.1:n.137+14691T>C
NR_130920.1:n.137+14691T>C
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