Canonical Allele Identifier: CA775632298

Gene:

Linked Data

• dbSNP Id: rs1260575302
• MyVariant Identifiers: chr17:g.8040790del (hg19) ; chr17:g.8137472del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8137472del , CM000679.2:g.8137472del	GRCh38
NC_000017.10:g.8040790del , CM000679.1:g.8040790del	GRCh37
NC_000017.9:g.7981515del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934202.1:n.183-1377del
XR_934203.1:n.70-2005del
XR_934202.2:n.414-1377del