Canonical Allele Identifier: CA2255111846
Gene:

Linked Data

dbSNP Id: rs1907310876

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237170del , CM000679.2:g.30237170del GRCh38
NC_000017.10:g.28564188del , CM000679.1:g.28564188del GRCh37
NC_000017.9:g.25588314del NCBI36
NG_011747.2:g.3772del

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+100del
XR_001752824.1:n.280+100del