Canonical Allele Identifier: CA982865628
Gene:

Linked Data

dbSNP Id: rs1907313151

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237214_30237257del , CM000679.2:g.30237214_30237257del GRCh38
NC_000017.10:g.28564232_28564275del , CM000679.1:g.28564232_28564275del GRCh37
NC_000017.9:g.25588358_25588401del NCBI36
NG_011747.2:g.3691_3734del

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+144_165+187del
XR_001752824.1:n.280+144_280+187del