Canonical Allele Identifier: CA2255111990
Gene:

Linked Data

dbSNP Id: rs1907322869

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237305_30237312del , CM000679.2:g.30237305_30237312del GRCh38
NC_000017.10:g.28564323_28564330del , CM000679.1:g.28564323_28564330del GRCh37
NC_000017.9:g.25588449_25588456del NCBI36
NG_011747.2:g.3625_3632del

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+235_165+242del
XR_001752824.1:n.280+235_280+242del