Canonical Allele Identifier: CA727900798

Gene:

Linked Data

• dbSNP Id: rs1293122073
• gnomAD v3: 17-30237175-TG-T
• gnomAD v4: 17-30237175-TG-T
• MyVariant Identifiers: chr17:g.28564194del (hg19) ; chr17:g.30237176del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30237181del , CM000679.2:g.30237181del	GRCh38
NC_000017.10:g.28564199del , CM000679.1:g.28564199del	GRCh37
NC_000017.9:g.25588325del	NCBI36
NG_011747.2:g.3761del

Transcript Alleles

HGVS	Amino-acid Change
XR_934654.1:n.165+111del
XR_001752824.1:n.280+111del