Canonical Allele Identifier: CA847393003
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1179575826
MyVariant Identifiers: chr8:g.130613695_130613716del (hg19) chr8:g.129601449_129601470del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601449_129601470del , CM000670.2:g.129601449_129601470del GRCh38
NC_000008.10:g.130613695_130613716del , CM000670.1:g.130613695_130613716del GRCh37
NC_000008.9:g.130682877_130682898del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78458_312+78479del
Search 100 bp 5'
Search 100 bp 3'