Canonical Allele Identifier: CA727901100

Gene:

Linked Data

• dbSNP Id: rs1283533954
• MyVariant Identifiers: chr17:g.28564346_28564347insG (hg19) ; chr17:g.30237328_30237329insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.30237333dup , CM000679.2:g.30237333dup	GRCh38
NC_000017.10:g.28564351dup , CM000679.1:g.28564351dup	GRCh37
NC_000017.9:g.25588477dup	NCBI36
NG_011747.2:g.3608dup

Transcript Alleles

HGVS	Amino-acid Change
XR_934654.1:n.165+263dup
XR_001752824.1:n.280+263dup