Canonical Allele Identifier: CA2255112000
Gene:

Linked Data

dbSNP Id: rs1907324275

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237311_30237313del , CM000679.2:g.30237311_30237313del GRCh38
NC_000017.10:g.28564329_28564331del , CM000679.1:g.28564329_28564331del GRCh37
NC_000017.9:g.25588455_25588457del NCBI36
NG_011747.2:g.3624_3626del

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+241_165+243del
XR_001752824.1:n.280+241_280+243del