Canonical Allele Identifier: CA2255111923
Gene:

Linked Data

dbSNP Id: rs1907315705

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237244_30237246del , CM000679.2:g.30237244_30237246del GRCh38
NC_000017.10:g.28564262_28564264del , CM000679.1:g.28564262_28564264del GRCh37
NC_000017.9:g.25588388_25588390del NCBI36
NG_011747.2:g.3691_3693del

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+174_165+176del
XR_001752824.1:n.280+174_280+176del