Canonical Allele Identifier: CA296568437

Gene:

Linked Data

• dbSNP Id: rs35612601
• MyVariant Identifiers: chr18:g.10321186_10321187insG (hg19) ; chr18:g.10321189_10321190insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10321189_10321190insG , CM000680.2:g.10321189_10321190insG	GRCh38
NC_000018.9:g.10321186_10321187insG , CM000680.1:g.10321186_10321187insG	GRCh37
NC_000018.8:g.10311186_10311187insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935138.1:n.665+958_665+959insC
XR_001753344.1:n.650+958_650+959insC
XR_001753345.1:n.931_932insC
XR_001753346.1:n.549+958_549+959insC