Canonical Allele Identifier: CA1122483686
Gene:

Linked Data

dbSNP Id: rs1819678345

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551514_25551515insCCTTTTACAGCCTTTTACCG , CM000671.2:g.25551514_25551515insCCTTTTACAGCCTTTTACCG GRCh38
NC_000009.11:g.25551512_25551513insCCTTTTACAGCCTTTTACCG , CM000671.1:g.25551512_25551513insCCTTTTACAGCCTTTTACCG GRCh37
NC_000009.10:g.25541512_25541513insCCTTTTACAGCCTTTTACCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-942_50-941insGGTAAAAGGCTGTAAAAGGC
XR_929525.2:n.674-942_674-941insGGTAAAAGGCTGTAAAAGGC