Canonical Allele Identifier: CA919823929
Gene:

Linked Data

dbSNP Id: rs1567826436

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237266_30237308del , CM000679.2:g.30237266_30237308del GRCh38
NC_000017.10:g.28564284_28564326del , CM000679.1:g.28564284_28564326del GRCh37
NC_000017.9:g.25588410_25588452del NCBI36
NG_011747.2:g.3629_3671del

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+196_165+238del
XR_001752824.1:n.280+196_280+238del