Canonical Allele Identifier: CA982866221
Gene:

Linked Data

dbSNP Id: rs1907319253

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237282_30237309del , CM000679.2:g.30237282_30237309del GRCh38
NC_000017.10:g.28564300_28564327del , CM000679.1:g.28564300_28564327del GRCh37
NC_000017.9:g.25588426_25588453del NCBI36
NG_011747.2:g.3628_3655del

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+212_165+239del
XR_001752824.1:n.280+212_280+239del