Canonical Allele Identifier: CA856539057

Gene:

Linked Data

• dbSNP Id: rs1285275652
• MyVariant Identifiers: chr8:g.89547963_89547964insT (hg19) ; chr8:g.88535734_88535735insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88535741dup , CM000670.2:g.88535741dup	GRCh38
NC_000008.10:g.89547970dup , CM000670.1:g.89547970dup	GRCh37
NC_000008.9:g.89617086dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745651.2:n.1673+10782dup
XR_001745653.2:n.286-6939dup
XR_928383.3:n.1475+10782dup