Canonical Allele Identifier: CA625447449

Gene:

Linked Data

• dbSNP Id: rs1386262256
• gnomAD v2: 17-28564302-CTGGGGGTG-C
• gnomAD v3: 17-30237284-CTGGGGGTG-C
• gnomAD v4: 17-30237284-CTGGGGGTG-C
• MyVariant Identifiers: chr17:g.28564303_28564310del (hg19) ; chr17:g.30237285_30237292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30237285_30237292del , CM000679.2:g.30237285_30237292del	GRCh38
NC_000017.10:g.28564303_28564310del , CM000679.1:g.28564303_28564310del	GRCh37
NC_000017.9:g.25588429_25588436del	NCBI36
NG_011747.2:g.3645_3652del

Transcript Alleles

HGVS	Amino-acid Change
XR_934654.1:n.165+215_165+222del
XR_001752824.1:n.280+215_280+222del