Canonical Allele Identifier: CA563611903
Gene: CCDC69 HGNC NCBI

Linked Data

dbSNP Id: rs1262951882

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151206370T>C , CM000667.2:g.151206370T>C GRCh38
NC_000005.9:g.150585931T>C , CM000667.1:g.150585931T>C GRCh37
NC_000005.8:g.150566124T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000355417.7:c.49-895A>G MANE Select ENSP00000347586.2:n.49-895A>G
ENST00000355417.6:c.49-895A>G ENSP00000347586.2:n.49-895A>G
ENST00000521308.5:n.172-4682A>G
ENST00000522179.1:n.491-895A>G
NM_015621.2:c.49-895A>G NP_056436.2:n.49-895A>G
NM_015621.3:c.49-895A>G MANE Select NP_056436.2:n.49-895A>G