Canonical Allele Identifier: CA186000969

Gene: CCDC26

Linked Data

• dbSNP Id: rs924464273
• MyVariant Identifiers: chr8:g.130613737G>T (hg19) ; chr8:g.129601491G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129601491G>T , CM000670.2:g.129601491G>T	GRCh38
NC_000008.10:g.130613737G>T , CM000670.1:g.130613737G>T	GRCh37
NC_000008.9:g.130682919G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.312+78437C>A