Canonical Allele Identifier: CA651969881

Gene:

Linked Data

• dbSNP Id: rs1469735727
• COSMIC: COSN23030051
• MyVariant Identifiers: chr7:g.123946350_123946351insT (hg19) ; chr7:g.124306296_124306297insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.124306303dup , CM000669.2:g.124306303dup	GRCh38
NC_000007.13:g.123946357dup , CM000669.1:g.123946357dup	GRCh37
NC_000007.12:g.123733593dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956584.1:n.73-175dup