Canonical Allele Identifier: CA676911615

Gene:

Linked Data

• dbSNP Id: rs1340610477
• MyVariant Identifiers: chr11:g.45528035_45528036insCA (hg19) ; chr11:g.45506485_45506486insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45506487_45506488dup , CM000673.2:g.45506487_45506488dup	GRCh38
NC_000011.9:g.45528037_45528038dup , CM000673.1:g.45528037_45528038dup	GRCh37
NC_000011.8:g.45484613_45484614dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001748204.2:n.909-16716_909-16715dup
XR_931245.3:n.566-16716_566-16715dup