Canonical Allele Identifier: CA846958859

Gene:

Linked Data

• dbSNP Id: rs1188946938
• MyVariant Identifiers: chr8:g.126490564_126490565insG (hg19) ; chr8:g.125478322_125478323insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478323dup , CM000670.2:g.125478323dup	GRCh38
NC_000008.10:g.126490565dup , CM000670.1:g.126490565dup	GRCh37
NC_000008.9:g.126559747dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5009dup